Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0917816 (mental retardation)
15,867 document(s) hit in 31,850,051 MEDLINE articles (0.01 seconds) .

Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .
Human Gene/Protein
FMR1 0.008
X-linked 0.006
FMRP 0.004
fragile X mental retardation protein 0.003
MRX 0.003
WAGR 0.003
aniridia 0.002
Rubinstein-Taybi syndrome 0.001
FRAXE 0.001
FMR2 0.001
ATRX 0.001
fatty aldehyde dehydrogenase 0.001
FMR1 protein 0.001
Rett syndrome 0.001
FXR2P 0.001
chromosome 21 0.001
XLMR 0.001
ATRX protein 0.001
MECP2 0.001
MASA 0.001
IL1RAPL1 0.001
FXR1P 0.001
PAK3 0.001
Smith-Lemli-Opitz syndrome 0.001
ARX 0.001
X-linked recessive 0.001
Aristaless-related homeobox 0.001
OPHN1 0.001
SLC6A8 0.001
XNP 0.001
OCRL1 0.001
PQBP1 0.001
FXR2 0.000
VCX-A 0.000
oligophrenin-1 0.000
FXR1 0.000
FISH 0.000
ZFHX1B 0.000
Sotos syndrome 0.000
FACL4 0.000
ARHGEF6 0.000
creatine transporter 0.000
HOPA 0.000
protocadherin 19 0.000
p11 0.000
Fragile X Mental Retardation Protein 0.000
TM4SF2 0.000
RPS6KA3 0.000
PQBP-1 0.000
MIM 0.000
PHF8 0.000
IL1RAPL2 0.000
JARID1C 0.000
MRX30 0.000
MRX9 0.000
PIGV 0.000
L1CAM 0.000
ALDH3A2 0.000
RSK2 0.000
DAXX 0.000
Dymeclin 0.000
DXS6673E 0.000
p21-activated kinase 3 0.000
X-linked) 0.000
CUL4B 0.000
CC2D1A 0.000
alphaPIX 0.000
X-chromosome 0.000
RNA-binding protein 0.000
TSC2 0.000
CLP36 0.000
TSC1 0.000
MCPH1 0.000
FTSJ1 0.000
VCX-C 0.000
MRXS3 0.000
NHS protein 0.000
VCX-B1 0.000
retinoic acid induced 1 0.000
strabismus 0.000
NIPBL 0.000
oligophrenin 1 0.000
DAXX protein 0.000
PCDH19 0.000
DYRK1A 0.000
PHD finger protein 8 0.000
neurotrypsin 0.000
CLN8 0.000
C7orf11 0.000
239FB 0.000
ZNF261 0.000
Nance-Horan syndrome 0.000
C21orf5 0.000
POMT1 0.000
CDKL5 0.000
RSH 0.000
PIGO 0.000
ZNF81 0.000
LAF4 0.000
L1 cell adhesion molecule 0.000
RAI1 0.000
ZNF258 0.000
ZNF41 0.000
MRX45 0.000
VCX-B 0.000
Microcephalin 0.000
UBE3A 0.000
PGAP3 0.000
NSD1 0.000
fukutin-related protein 0.000
ZNF711 0.000
p13 0.000
fukutin 0.000
p22 0.000
BBS4 0.000
AP1S2 0.000
TBC1D24 0.000
BBS3 0.000
PIGL 0.000
BBS1 0.000
COH1 0.000
XLIS 0.000
PKU 0.000
BBS2 0.000
GDP-dissociation inhibitor 0.000
tuberin 0.000
UHX1 0.000
MCPH5 0.000
ocrl1 0.000
TTDN1 0.000
CRASH 0.000
VCX3A 0.000
POMT2 0.000
VCX 0.000
prolidase 0.000
Oculocerebrorenal syndrome of Lowe 0.000
aspartylglucosaminidase 0.000
LIS1 0.000
PGAP2 0.000
SLC12A6 0.000
telomeric 0.000
SMCX 0.000
MRX34 0.000
PRSS12 0.000
SIL1 0.000
OCRL 0.000
WRP 0.000
lysosome-associated membrane protein-2 0.000
transmembrane and coiled-coil domains 1 0.000
Rho guanine nucleotide exchange factor 6 0.000
LGMD2K 0.000
NUFIP1 0.000
UPF3B protein 0.000
NLGN4X 0.000
srGAP3 0.000
guanidinoacetate methyltransferase 0.000
KIAA1718 0.000
C2orf37 0.000
GRIA3 0.000
X-linked protein 0.000
trichothiodystrophy 0.000
SNF2 0.000
CENPJ 0.000
KH2 0.000
PAFAH1B3 protein 0.000
Phospholipase DDHD2 0.000
DXS164 0.000
ZNF630 0.000
PIGX 0.000
OPHN1 protein 0.000
MAM domain containing 2 0.000
MORN repeat containing 4 0.000
methyl-CpG binding domain protein 5 0.000
RhoGAP2 0.000
MRPS14 0.000
Homer 1 variant 0.000
SYNE1 protein 0.000
C14orf23 0.000
ISSX 0.000
WHSC1 protein 0.000
glutamate receptor, ionotropic, N-methyl D-aspartate 1 0.000
LYSMD3 0.000
FLJ20344 0.000
ADRACALIN 0.000
HADH2 protein 0.000
CASKIN1 0.000
Cytochrome b5 reductase 3 0.000
RBBP7 protein 0.000
tissue plasminogen activator precursor 0.000
GDF10 protein 0.000
WD repeat-containing protein 81 0.000
LOC442459 0.000
variable charge, X chromosome 0.000
HSA272195 0.000
COX4NB 0.000
transient receptor potential cation channel, subfamily M, member 3 0.000
ZNF271 0.000
NHSL2 0.000
praja 1 0.000
AMMECR1 0.000
FLJ25076 0.000
MRX59 0.000
glycine amidinotransferase 0.000
GDI-1 0.000
KIR4.2 0.000
239AB 0.000
ZNF124 0.000
FXR1 protein 0.000
arylsulfatase E 0.000
DSCR1 0.000
PEPD 0.000
cystathionine beta-synthase 0.000
PAX6 0.000
ESCO2 0.000
GAMT 0.000
SLC9A7 0.000
WHSC2 0.000
She 0.000
methyl-CpG binding protein 2 0.000
MKKS 0.000
UBE2A 0.000
collybistin 0.000
McKusick-Kaufman syndrome 0.000
CDK5RAP2 0.000
ATR 0.000
KIAA1202 0.000
U5-15kD 0.000
monocarboxylate transporter 8 0.000
hypoxanthine-guanine phosphoribosyltransferase 0.000
SIZN1 0.000
SCML1 0.000
Xg blood group 0.000
TSPAN6 0.000
methyl CpG binding protein 2 0.000
phenylalanine hydroxylase 0.000
CDT 0.000
WDR81 0.000
SMC1A 0.000
ATP8A2 0.000
DMD 0.000
GMPPA 0.000
ZNF252 0.000
FAM120C 0.000
Microfibril-associated glycoprotein 4 0.000
KIAA0136 0.000
SCO cytochrome oxidase deficient homolog 2 (yeast) 0.000
hZFH 0.000
KSP37 0.000
Myosin regulatory light chain interacting protein 0.000
dystrophin C-terminal region 0.000
EVI2A 0.000
CALL 0.000
ARHGDIG 0.000
UROC1 0.000
FLJ20071 0.000
enkurin 0.000
BBS5 0.000
myosin IXA 0.000
PEX12 protein 0.000
KIAA0958 0.000
TTLL11 0.000
KIAA1185 0.000
SNAPC3 0.000
ZDHHC15 0.000
X-linked neuroligin 4 0.000
CINAP 0.000
WS-betaTRP 0.000
KIAA0215 0.000
phenylalanine Hydroxylase 0.000
NAP1L3 0.000
Mrps18a 0.000
CLK2 protein 0.000
Oligophrenin 1 0.000
SRCAP protein 0.000
FLJ22729 0.000
ASFMR1 0.000
CYFIP1 0.000
MRI 0.000
aspartylglycosaminuria 0.000
dentatorubral-pallidoluysian atrophy 0.000
CLN5 0.000
EVI2B 0.000
DLG3 0.000
SPG15 0.000
CREBBP 0.000
cryptic 0.000
NXF5 0.000
epithelial cell transforming 2 0.000
IL-1R9 0.000
ornithine transporter 0.000
SPG11 0.000
TRKA 0.000
VCFS 0.000
elastin gene 0.000
SLC16A2 0.000
Fukuyama-type congenital muscular dystrophy 0.000
cell death inhibiting RNA 0.000
GRIK4 0.000
KIAA1840 0.000
AP19 0.000
EIF4H 0.000
WT1 0.000
inositol polyphosphate-5-phosphatase 0.000
FKIF2 0.000
PTPN11 protein 0.000
AP1B1 0.000
OCRL-1 protein 0.000
VSTM2B 0.000
C6orf217 0.000
CSHL1 0.000
KIAA0179 0.000
PCMTD2 0.000
MG21 0.000
septin 11 0.000
TAFA2 0.000
CAF1A 0.000
F8c 0.000
PTD004 0.000
ZDHHC12 0.000
FLJ23560 0.000
ZBTB7C 0.000
LINS1 0.000
TMPRSS5 0.000
Dmx-like 2 0.000
NAP1L 0.000
UPF3X 0.000
SLC9A6 0.000
VPS13B 0.000
NPHP1 0.000
RNA binding protein 0.000
merosin 0.000
AN2 0.000
ARHGEF9 0.000
Aspartylglycosaminuria 0.000
RSK4 0.000
CASK 0.000
KCNAB2 0.000
rabconnectin 0.000
E6-AP ubiquitin-protein ligase 0.000
ZNF674 0.000
PJA1 0.000
FALDH 0.000
dystrophin gene 0.000
OFD 0.000
TBCE 0.000
NLGN3 0.000
dystrophin 0.000
Mol 0.000
SMC3 0.000
POMGnT1 0.000
F8C 0.000
OTUD7A 0.000
GTG 0.000
adenylosuccinate lyase 0.000
metabotropic glutamate receptor 0.000
tolloid-like protein 0.000
EFCAB2 0.000
TRAF family member-associated NF-kappa-B activator 0.000
SMC1A protein 0.000
NFIX protein 0.000
WBSCR1 0.000
spinesin 0.000
ZNF397 0.000
aristaless-like homeobox 4 0.000
ZNF396 0.000
zinc finger protein 638 0.000
KIAA0226 0.000
RAB9B 0.000
CXorf56 0.000
ornithine aminotransferase-like 1 0.000
ZNF182 0.000
Neurodap1 0.000
C20orf133 0.000
plexin B3 0.000
DEP domain containing 5 0.000
METRNL 0.000
HNRPU 0.000
SLC6A10P 0.000
BFLS 0.000
JARID1C protein 0.000
PLCH2 0.000
SIP1 0.000
HHH 0.000
PHD domain 0.000
MRPP2 0.000
CDH9 0.000
choroideremia 0.000
DEHAL1 0.000
REPS2 0.000
CASC5 0.000
ZFYVE26 0.000
CHRNA7 0.000
p23 0.000
NTRK1 0.000
Caytaxin 0.000
CEP152 0.000
ASPM 0.000
UBR1 0.000
ACSL4 0.000
PAFAH1B3 0.000
VCY 0.000
ZNF335 0.000
MPS IIIB 0.000
STIL 0.000
AHI1 0.000
HRAS 0.000
LAMP-2 0.000
KAL1 0.000
CYFIP2 0.000
ALX4 0.000
DCX 0.000
Smad-interacting protein 1 0.000
MLL2 protein 0.000
PJA2 0.000
HEPACAM2 0.000
TRAPPC9 0.000
chromodomain helicase DNA binding protein 2 0.000
K-Cl cotransporter 3 0.000
SESTD1 0.000
DSCR1L2 0.000
retinophilin 0.000
ARD1A 0.000
lacking exon 14 0.000
PDZD4 0.000
ZNF157 0.000
SGN3 0.000
ATLD 0.000
P54NRB 0.000
DSCR4 0.000
CCDC28B 0.000
RTN4IP1 0.000
Pbx regulating protein 1 0.000
MG44 0.000
ZNF536 0.000
ASPA protein 0.000
MLLT2 0.000
PTCD3 0.000
LPHN1 0.000
FRA10A 0.000
SNRPN 0.000
SMC1alpha 0.000
C21orf2 0.000
GTF2IRD2 0.000
PCDH8 0.000
POU3F4 0.000
PYCR1 0.000
L1 gene 0.000
SHANK3 0.000
thyroid hormone 0.000
p12 0.000
SPG2 0.000
CA8 0.000
NCAPG2 0.000
ATP1A2 0.000
Sep 0.000
NLGN1 0.000
TRK1 0.000
DAG 0.000
acid alpha-glucosidase 0.000
KNP1 0.000
FSP2 0.000
MRT1 0.000
DSCR6 0.000
RAD23 homolog B 0.000
AUTS2 protein 0.000
ARIP4 0.000
ZNF592 0.000
PROSAP2 0.000
MBD3 protein 0.000
SREB3 0.000
OCRL protein 0.000
dual oxidase maturation factor 2 0.000
TrpC5 0.000
STIL protein 0.000
MRPL43 0.000
JARID1D 0.000
SEN34 0.000
Transducin-like enhancer protein 1 0.000
KPTN 0.000
ZNF6 0.000
homer 1 0.000
GTP-binding protein 2 0.000
EVR1 0.000
THY28 0.000
MTMR10 0.000
LRFN5 0.000
cooperator of PRMT5 0.000
RLA1 0.000
Acyl-CoA synthetase long-chain family member 4 0.000
NRXN1 0.000
KCNJ10 0.000
WHSC1 0.000
GTF2I 0.000
NHE6 0.000
PWS 0.000
MPS IIIA 0.000
MPS II 0.000
KIAA2022 0.000
IR10 0.000
delta-catenin 0.000
SC5D 0.000
AGTR2 0.000
cell adhesion molecule L1 0.000
PCTK1 0.000
CGGBP1 0.000
STRP 0.000
p15 0.000
lysosomal sialidase 0.000
SLC17A5 0.000
DSCR 0.000
GTF2IRD1 0.000
spermine synthase 0.000
DPM3 0.000
glypican 1 0.000
SECISBP2 0.000
ZDHHC9 0.000
INPP5B 0.000
PHC1 0.000
NUFIP2 0.000
cytokine receptor-like factor 3 0.000
PAHX-AP1 0.000
cystatin-like molecule 0.000
PRRG4 0.000
SEZ6L2 0.000
MORG1 0.000
TUSC5 0.000
PPEF1 0.000
DIP2B 0.000
WDR73 0.000
hydrometrocolpos 0.000
NKX2-6 0.000
Dopamine receptor D4 0.000
9p22 0.000
FGS 0.000
steroid sulfatase 0.000
neurofibromatosis 0.000
BBS7 0.000
RBS 0.000
Rab3-GAP 0.000
PIG-B 0.000
LRRN1 0.000
CACNA1A 0.000
KH1 0.000
UPF3B 0.000
PEX7 0.000
SSADH 0.000
STXBP1 0.000
MAOB 0.000
FSHB 0.000
WDR62 0.000
CTIP1 0.000
PTPN11 0.000
IL-1 receptor accessory protein 0.000
glycerol kinase 0.000
DNMT3B 0.000
mGluR5 0.000
NHSL1 0.000
MYO9A 0.000
SLC8A2 0.000
sodium leak channel, non-selective 0.000
LRCH1 0.000
ENOPH1 0.000
inositol polyphosphate-5-phosphatase E 0.000
TSC1 protein 0.000
PCDH11 0.000
HADH2 0.000
Tetraspanin-7 0.000
ALO17 0.000
monocarboxylate transporter 12 0.000
ANKLE2 0.000
punctin 0.000
SASS6 0.000
Tudor domain-containing protein 3 0.000
LARGE 0.000
HIP14L 0.000
MAB21L1 0.000
aspartoacylase 0.000
BBS 0.000
CUL4A 0.000
Freud-1 0.000
EP300 0.000
SMEI 0.000
NIPA2 0.000
CRT2 0.000
BBS12 0.000
teneurin-1 0.000
CHL1 0.000
SLC4A4 0.000
sterol 27-hydroxylase 0.000
STX1A 0.000
MED12 0.000
AFF2 0.000
MFAP4 0.000
iodotyrosine deiodinase 0.000
TUSC3 0.000
BCL-6 corepressor 0.000
MKRN3 0.000
lysosomal alpha-mannosidase 0.000
RNF180 0.000
PSG4 0.000
METAP2 0.000
LYC5 0.000
BTR1 0.000
WDR13 0.000
FRMPD4 0.000
axonal transport of synaptic vesicles 0.000
GARS-AIRS-GART 0.000
M/SCHAD 0.000
NANH 0.000
ZNF21 0.000
MTND6 0.000
Dyrk3 0.000
RAB26 0.000
MLC-2A 0.000
PCQAP 0.000
GLUR2 0.000
WIT1 0.000
FLNA protein 0.000
CNKSR2 0.000
CAPN6 0.000
ATPIF1 0.000
SPPL2c 0.000
SLC25A43 0.000
PHD zinc finger 0.000
GNB5 0.000
PHF6 0.000
KCTD11 0.000
GLUD1 0.000
CRBN 0.000
MAP2K2 0.000
WHS 0.000
TRPS1 0.000
LHFPL3 0.000
FHF2 0.000
RAY1 0.000
PREB 0.000
BMP-3b 0.000
cereblon 0.000
FAM36A 0.000
LECT1 0.000
ATIP1 0.000
FHL1B 0.000
BLMH 0.000
NCAPD3 0.000
ARHGAP11A 0.000
CRTR 0.000
pitrilysin metallopeptidase 1 0.000
ARCL 0.000
OCRL-1 0.000
KIAA1018 0.000
CD125 0.000
Serine proteinase inhibitor 0.000
Formiminotransferase-cyclodeaminase 0.000
short coiled coil protein 0.000
GST-5 0.000
centrosomal P4.1-associated protein 0.000
BBS8 0.000
Down syndrome cell adhesion molecule 0.000
RP11 0.000
UTR 0.000
SWI2 0.000
HSD10 0.000
DYNC1H1 0.000
VLDLR 0.000
ZIC4 0.000
PIG-M 0.000
DPM2 0.000
CLN7 0.000
SCN1A 0.000
IP1 0.000
6-pyruvoyltetrahydropterin synthase 0.000
protein O-mannosyltransferase 0.000
Phosphoglycerate kinase 0.000
MNB 0.000
RAB3A 0.000
KDM6A 0.000
RA-GEF 0.000
CDH7 0.000
CDKL3 0.000
NAALADL2 0.000
GKD 0.000
alpha-centractin 0.000
Kruppel-like factor 8 0.000
PCDH12 0.000
KCNK17 0.000
CRYA1 0.000
RABL2B 0.000
HACS1 0.000
ZNF179 0.000
GTF2H5 0.000
CMTX5 0.000
WD repeat domain 7 0.000
SGCZ 0.000
ARMC4 0.000
SET binding protein 1 0.000
KIAA1279 0.000
CDH18 0.000
PAHX 0.000
MIFR 0.000
ZAKI-4 0.000
DMXL2 0.000
LARP 0.000
SNX19 0.000
CTTNBP2 0.000
GSE1 0.000
Succinic semialdehyde dehydrogenase 0.000
HSD17B10 0.000
ARSA 0.000
succinic semialdehyde dehydrogenase 0.000
ATP6V1B2 0.000
ALAS2 0.000
DAX1 0.000
RELN 0.000
LAMA2 0.000
axonal 0.000
Beckwith-Wiedemann syndrome 0.000
DDHD2 0.000
FHM2 0.000
SPTBN2 0.000
PCDH17 0.000
choline kinase beta 0.000
galactose-1-phosphate uridyltransferase 0.000
ITPR1 0.000
TB3-1 0.000
CC2D1B 0.000
TTC8 0.000
AHDC1 0.000
USP32 0.000
PSG3 0.000
MHAT 0.000
SUGT1 0.000
TPRC 0.000
MCCC2 0.000
TIAF1 0.000
EVX2 0.000
RASGEF1B 0.000
BMP2K 0.000
LETM1 0.000
catenin beta-1 0.000
ASC2 0.000
mnb 0.000
CRYA2 0.000
BRAG1 0.000
ZNF198 0.000
isocitrate dehydrogenase 1 0.000
M6b 0.000
PAX6 protein 0.000
OATL1 0.000
AGAT 0.000
Rho 0.000
ADHD 0.000
P5C 0.000
FRAS1 0.000
Kir5.1 0.000
CUL4 0.000
ARHGEF7 0.000
JJAZ1 0.000
NRXN2 0.000
Cullin 4B 0.000
GPS2 0.000
ACTG1 0.000
SOX8 0.000
Facioscapulohumeral muscular dystrophy 0.000
panhypopituitarism 0.000
MID1 0.000
B(0)AT1 0.000
CHRNA4 0.000
p25 0.000
NLGN4Y 0.000
YF5 0.000
TPRD 0.000
PCDH20 0.000
GTPBP2 0.000
MAGE-D 0.000
PIK4CA 0.000
RPS8 0.000
MAGED2 0.000
Fibrillin 1 0.000
neighbor of BRCA1 gene 1 0.000
ZNF74 0.000
NEUROD6 0.000
ACS4 0.000
Dystrophin protein 0.000
BRWD3 0.000
HNRNPH2 0.000
Silver syndrome 0.000
PIGN 0.000
NPAS3 0.000
PCDH9 0.000
small nuclear ribonucleoprotein polypeptide N 0.000
NXF 0.000
p14 0.000
inositol polyphosphate 5-phosphatase 0.000
alpha-L-iduronidase 0.000
ADSL 0.000
SIPP1 0.000
CC2D2A 0.000
GABRD 0.000
STS 0.000
ASG 0.000
Protocadherin 0.000
PAFAH1B1 0.000
NDE1 0.000
MEB 0.000
dynamin family member 0.000
CFTD 0.000
killer-specific secretory protein of 37 kDa 0.000
SVAS 0.000
ISO1 0.000
CCBE1 0.000
putative nuclear protein 0.000
PCTAIRE1 0.000
SCLT1 0.000
NUT2 0.000
NCAPH2 0.000
GMPPB 0.000
calmodulin-dependent protein kinase II alpha 0.000
SLC8A3 0.000
Urocanase 0.000
LIM domain only 1 0.000
forkhead box L2 0.000
CLN 0.000
GPR56 0.000
GAN 0.000
MSPL 0.000
ERCC8 0.000
alkyl-DHAP synthase 0.000
KCC3 0.000
EXT2 0.000
LINCL 0.000
Troyer syndrome 0.000
CNTN4 0.000
MANB 0.000
T-brain-1 0.000
GNAZ 0.000
DAB1 0.000
ZMYM3 0.000
TTC3 0.000
ALDH4 0.000
GCP5 0.000
BCR protein 0.000
PNPLA4 0.000
Golgi-associated ATPase enhancer of 16 kDa 0.000
CDH8 0.000
DCR2 0.000
TUBGCP5 0.000
GNG2 0.000
autism susceptibility candidate 2 0.000
PSD-95 0.000
MEK2 0.000
NDEL1 0.000
KMT2D 0.000
SPTAN1 0.000
DMPK 0.000
Y chromosome 0.000
KAT6A 0.000
very low density lipoprotein receptor 0.000
Fukutin-related protein 0.000
ABCX 0.000
PHD finger 0.000
CREB binding protein 0.000
CNTNAP2 0.000
MLL2 0.000
PARVB 0.000
FAM167A 0.000
LARK 0.000
SLC25A15 0.000
APBA2 0.000
MYM 0.000
SPON1 0.000
BCAS4 0.000
KANK 0.000
ARHGAP11B 0.000
BSCL2 0.000
PRRT2 0.000
IQSEC2 0.000
NGFB 0.000
p26 0.000
GRIK2 0.000
ELN 0.000
sorting nexin 3 0.000
Frizzled-4 0.000
OFD1 0.000
MAOA 0.000
POLR3G 0.000
POP4 0.000
VPS33A 0.000
TRNT1 0.000
ALG11 0.000
GSCL 0.000
ARHGEF4 0.000
PIG-C 0.000
KIF26B 0.000
myelin transcription factor 1 0.000
MED17 0.000
LARGE1 0.000
WDR60 0.000
CHD6 0.000
T-cell lymphoma invasion and metastasis 1 0.000
importin 13 0.000
FAM111A 0.000
PAFAH1B2 0.000
acyl-CoA synthetase 4 0.000
sorting nexin 17 0.000
transcription factor II H 0.000
alpha-N-acetylglucosaminidase 0.000
FGF13 0.000
PRS I 0.000
PCDH10 0.000
DOCK8 0.000
Cep290 0.000
FOXE1 0.000
biotinidase 0.000
phosphomannomutase 2 0.000
EFNB2 0.000
IL-18Rbeta 0.000
RFC2 0.000
SMCY 0.000
dihydropteridine reductase 0.000
neuroligin 2 0.000
DNMT3L 0.000
histone 0.000
PGK1 0.000
SFI1 0.000
PSP2 0.000
PIGH 0.000
alpha-1,2-mannosyltransferase 0.000
PTCHD1 0.000
RBM14 0.000
SLC25A5 0.000
PRDM12 0.000
CNK1 0.000
transmembrane transport protein 0.000
Exostosin-1 0.000
RASA3 0.000
SLC35C1 0.000
JMJD2C 0.000
PKCI 0.000
MACROD2 0.000
DLGAP2 0.000
ERCC6 0.000
Wilms' tumor gene 0.000
COL4A5 0.000
HRAS1 0.000
AF4 0.000
coagulation factor IX 0.000
dihydroxyacetone phosphate acyltransferase 0.000
HPRT 0.000
WWOX 0.000
MMACHC 0.000
TUBA1A 0.000
RAB3GAP1 0.000
MBD5 0.000
acid-sensing ion channel 2 0.000
OA1 0.000
E-Syt2 0.000
CKAP2 0.000
BCL7B 0.000
cullin 4B 0.000
ARHGEF3 0.000
putative zinc finger transcription factor 0.000
AARS 0.000
HM5 0.000
DLG1 0.000
DSCAM 0.000
COQ4 0.000
retinoic acid-induced protein 0.000
GPI1 0.000
ARAF1 0.000
p58.1 0.000
CDX4 0.000
MRPP3 0.000
HOXA6 0.000
UNC80 0.000
CREB-binding protein 0.000
p36 0.000
CDL 0.000
neurofibromatosis type 1 0.000
CTNND2 0.000
DLG4 0.000
DCR 0.000
LAD2 0.000
CLN1 0.000
ADNP 0.000
E6-AP 0.000
SPG3 0.000
SGCB 0.000
SLC16A12 0.000
FTCD 0.000
GRAF 0.000
MPP7 0.000
T-cell immune regulator 1 0.000
AC19 0.000
Dopamine D4 receptor 0.000
TSPYL5 0.000
GALK 0.000
Dyrk2 0.000
oculocutaneous albinism II 0.000
DNAI2 0.000
GPHN 0.000
protein O-fucosyltransferase 2 0.000
putative GTP-binding protein 0.000
Cep135 0.000
NADH cytochrome b5 reductase 0.000
lamp-2 0.000
RhoGAP 0.000
TCF4 0.000
LAMP2 0.000
PMM2 0.000
NEU1 0.000
WD repeat-containing protein 5 0.000
FEZ 0.000
DDX39 0.000
NXF2 0.000
Ymer 0.000
SCML2 0.000
CEP131 0.000
tumor suppressor candidate 3 0.000
rap1GAP 0.000
coxsackie virus and adenovirus receptor 0.000
mitogen-activated protein kinase kinase kinase 3 0.000
SCN3A 0.000
Sra-1 0.000
LRRTM2 0.000
Tbr-1 0.000
MAP1B protein 0.000
FBXL10 0.000
Cenexin 0.000
PORC 0.000
ATP6AP1 0.000
TBCD 0.000
LCA5 0.000
CACNB4 0.000
Spred-1 0.000
MBNL1 protein 0.000
PTPRZ 0.000
PDE6D 0.000
POLR3A 0.000
SYNGAP1 0.000
SGCE 0.000
HSAN 0.000
AAAS 0.000
CA1 0.000
RAD26 0.000
neurexin 1 0.000
gephyrin 0.000
AVPR2 0.000
KSP 0.000
KDM5C 0.000
GNAS 0.000
MID2 0.000
NIPA1 0.000
EHMT1 0.000
PDS5 0.000
progressive ankylosis protein 0.000
MAPK8IP1 0.000
ARFGAP1 0.000
Misu 0.000
CDH10 0.000
TSPAN7 0.000
alpha thalassemia/mental retardation syndrome X-linked 0.000
RPL6 0.000
Apolipoprotein E receptor 2 0.000
plasma membrane proteolipid 0.000
equilibrative nucleoside transporter 2 0.000
Protocadherin-1 0.000
SLC4A10 0.000
PRKX 0.000
ARFGEF2 0.000
NBCe1 0.000
NRXN3 0.000
CBP 0.000
GLI3 0.000
SHANK2 0.000
cullin 0.000
FKBP6 0.000
Gemin4 0.000
Pyrroline-5-carboxylate reductase 0.000
ITSN 0.000
ATP2B2 0.000
BRX 0.000
brefeldin A-inhibited 0.000
AMIGO2 0.000
FXR 0.000
p21 0.000
sarcosine dehydrogenase 0.000
AIFM1 0.000
GART 0.000
carbonic anhydrase II 0.000
DM1 0.000
4-hydroxyphenylpyruvate dioxygenase 0.000
HYOU1 0.000
MPS IIIC 0.000
phytanoyl-CoA 2-hydroxylase 0.000
CAPN5 0.000
NKRF 0.000
renin receptor 0.000
DND1 0.000
PCWH 0.000
GORAB 0.000
Coronin-1A 0.000
RP13 0.000
affixin 0.000
FMN2 0.000
LIMK1 0.000
MEIS2 0.000
N33 0.000
CA II 0.000
ICD 0.000
CMG 0.000
sulfite oxidase 0.000
HRD 0.000
helicase II 0.000
Bravo 0.000
Huntingtin-interacting protein 1 0.000
RHAG 0.000
Tim13 0.000
enhanced at puberty 1 0.000
ubiquitin protein ligase E3A 0.000
GINS2 0.000
CHRND 0.000
NUDC 0.000
CYB5A 0.000
AF5q31 0.000
LRPAP1 0.000
srGAP2 0.000
polymerase I and transcript release factor 0.000
ZRANB3 0.000
PHF2 0.000
DMAP1 0.000
3-methylglutaconyl-CoA hydratase 0.000
EGR4 0.000
BRAG2 0.000
CYP27A1 0.000
L1 protein 0.000
Pex7 0.000
DFNA5 0.000
novel gene 0.000
spastin 0.000
RHS 0.000
transcriptional repressor 0.000
Arylsulfatase A 0.000
COL4A6 0.000
KCNJ3 0.000
GLUR1 0.000
14-3-3 gamma 0.000
kinesin light chain 1 0.000
Neuropsin 0.000
RAD6A 0.000
DNA helicase B 0.000
Btf 0.000
CCDC98 0.000
KIFC3 0.000
ZDHHC8 0.000
Walker 0.000
PAK2 0.000
FGD1 0.000
EIF2AK3 0.000
GCG 0.000
CLN3 0.000
histone deacetylase 4 0.000
TASK-3 0.000
DYRK1B 0.000
UBE1 0.000
plasmolipin 0.000
6A8 0.000
PCLO 0.000
DOCK7 0.000
MYT1 0.000
KAL 0.000
IL5RA 0.000
LRRTM1 0.000
CDH12 0.000
ARSACS 0.000
neuroligin 3 0.000
Hyal-2 0.000
Noc2 0.000
CLN6 0.000
forkhead box P1 0.000
PRKD1 0.000
MOCS3 0.000
Golgi-localized protein 0.000
amyloid precursor protein 0.000
BCOR 0.000
aprataxin 0.000
NCS-1 0.000
SETMAR 0.000
septin 7 0.000
ATAD5 0.000
KIF3C 0.000
ERG-associated protein with SET domain 0.000
HCFC1 0.000
MRCK 0.000
DSC3 0.000
mediator complex subunit 12 0.000
HPS3 0.000
PRP9 0.000
NDRF 0.000
TGIF2 0.000
Daxx 0.000
Glypican-5 0.000
REEP1 0.000
translin 0.000
FOXL2 0.000
iduronate-2-sulfatase 0.000
DCoH 0.000
SIAH2 0.000
SCA8 0.000
FAT4 0.000
MAP1B 0.000
beta-dystrobrevin 0.000
EPM1 0.000
ALG2 0.000
Cep215 0.000
SPG6 0.000
PCBD 0.000
C1-tetrahydrofolate synthase 0.000
KLF8 0.000
TFDP1 0.000
spliceosomal protein 0.000
TBX22 0.000
AE4 0.000
KCNJ12 0.000
TOP3B 0.000
CACNA2D3 0.000
IMMP2L 0.000
ABC-C 0.000
cystathionine-beta-synthase 0.000
WDR5 0.000
Shank3 0.000
autosomal recessive) 0.000
MERRF 0.000
ELP4 0.000
RINT-1 0.000
spindle associated 0.000
WDFY3 0.000
meiotic recombination 11 0.000
NPL3 0.000
PDCD6 0.000
GRID2 0.000
ETS2 0.000
RBBP7 0.000
P2Y14 receptor 0.000
AR protein 0.000
LHX4 0.000
KRT1 0.000
TBX1 0.000
YWHAE 0.000
ACSL3 0.000
SHOC2 0.000
GTPase activating protein 0.000
vacuolar proton pump 0.000
DNASE1 0.000
CTL4 0.000
SOS-1 0.000
AIRS 0.000
PKAN 0.000
Progesterone receptor membrane component 1 0.000
RORB 0.000
LDHB 0.000
dGK 0.000
GPR48 0.000
PIR121 0.000
SMAD9 0.000
DPP6 0.000
THRA 0.000
WT1) 0.000
CT1 0.000
unknown function 0.000
HADH 0.000
nibrin 0.000
RAD21 0.000
ribonucleoprotein 0.000
AMBN 0.000
EFNA3 0.000
syntaxin-binding protein 1 0.000
neurofilament-light 0.000
SRGAP1 0.000
Doc2 0.000
BBS10 0.000
Disease
mental retardation 1.000
mental retardation 0.941
fragile X syndrome 0.017
severe mental retardation 0.004
moderate mental retardation 0.003
developmental delay 0.003
mild mental retardation 0.003
Down syndrome 0.003
epilepsy 0.002
autism 0.002
FRAXA 0.002
FRAXE 0.002
cerebral palsy 0.002
profound mental retardation 0.001
ATRX 0.001
macrocephaly 0.001
Rett syndrome 0.001
developmental disabilities 0.001
phenylketonuria 0.001
congenital hypothyroidism 0.001
Congenital hypothyroidism 0.001
Cohen syndrome 0.001
tuberous sclerosis 0.001
trisomy 0.001
Smith-Lemli-Opitz syndrome 0.001
Bardet-Biedl syndrome 0.001
Partington syndrome 0.001
KMS 0.001
X-linked hydrocephalus 0.001
ichthyosis 0.001
lissencephaly 0.001
Angelman syndrome 0.001
Williams syndrome 0.001
deafness 0.001
genetic disorder 0.001
Prolidase deficiency 0.001
hypogonadism 0.001
spastic diplegia 0.001
Danon disease 0.001
Lowe syndrome 0.001
Sotos syndrome 0.001
Costello syndrome 0.001
Cornelia de Lange syndrome 0.001
MRX2 0.001
FGS 0.000
spastic paraplegia 0.000
CLS 0.000
Laurence-Moon-Biedl syndrome 0.000
ichthyosis 0.000
HCG 0.000
Wolf-Hirschhorn syndrome 0.000
homocystinuria 0.000
blepharophimosis 0.000
pachygyria 0.000
49,XXXXY syndrome 0.000
self-injurious behavior 0.000
brachycephaly 0.000
MRX3 0.000
Seckel syndrome 0.000
Phenylketonuria 0.000
MRX30 0.000
Richner-Hanhart syndrome 0.000
EFMR 0.000
learning disability 0.000
Norrie disease 0.000
mental handicap 0.000
MRX19 0.000
MRX16 0.000
anhidrosis 0.000
alpha thalassemia 0.000
Gillespie syndrome 0.000
FAS 0.000
Lesch-Nyhan syndrome 0.000
Maternal phenylketonuria 0.000
MRX9 0.000
hyperphenylalaninemia 0.000
HSAN IV 0.000
monosomy 8p 0.000
delayed speech 0.000
hydrocephalus 0.000
brittle hair 0.000
18q- syndrome 0.000
Autism 0.000
Opitz 0.000
Ohdo blepharophimosis syndrome 0.000
FGS2 0.000
Acrocephalopolysyndactyly 0.000
PDD 0.000
3p- syndrome 0.000
partial monosomy 6q 0.000
choreoathetosis 0.000
failure to thrive 0.000
tetraplegia 0.000
cleft palate 0.000
Aspartylglucosaminuria 0.000
epidermal nevus syndrome 0.000
Sutherland-Haan syndrome 0.000
MRX43 0.000
MRX41 0.000
MRX47 0.000
MRX48 0.000
MCPH1 0.000
Iodine deficiency 0.000
WAGRO 0.000
AN2 0.000
FRAXF 0.000
EPMR 0.000
acrodysostosis 0.000
trisomy 9p 0.000
Allan-Herndon-Dudley syndrome 0.000
SWS 0.000
Rud syndrome 0.000
Neuhauser syndrome 0.000
deaf mutism 0.000
oxycephaly 0.000
Primary microcephaly 0.000
borderline mental retardation 0.000
CLN8 0.000
Lujan-Fryns syndrome 0.000
Martsolf syndrome 0.000
monosomy 10p 0.000
MRX21 0.000
M-CMTC 0.000
cri-du-chat syndrome 0.000
hypothyroidism 0.000
Coffin-Siris syndrome 0.000
thalassemia 0.000
Joubert syndrome 0.000
optic atrophy 0.000
Taybi 0.000
pseudohypoparathyroidism 0.000
Ramon syndrome 0.000
1q deletion syndrome 0.000
Trisomy 17 0.000
WT1 0.000
Dandy-Walker malformation 0.000
syndrome X 0.000
inv(X) 0.000
Andermann syndrome 0.000
monosomy 9p 0.000
Guanidinoacetate methyltransferase deficiency 0.000
encephalopathy 0.000
strabismus 0.000
diplegia 0.000
cutis laxa 0.000
FRA12A 0.000
trichothiodystrophy 0.000
APMR2 0.000
Sabinas syndrome 0.000
MRX53 0.000
MRX45 0.000
Pashayan-Pruzansky syndrome 0.000
MRX29 0.000
MRX46 0.000
Golabi-Ito-Hall syndrome 0.000
Fine-Lubinsky syndrome 0.000
Kapur-Toriello syndrome 0.000
Atkin-Flaitz syndrome 0.000
Deficiency of carbonic anhydrase 0.000
Carpenter syndrome 0.000
XLIS 0.000
craniosynostosis 0.000
Baraitser-Winter syndrome 0.000
SMS 0.000
tetrasomy 15q 0.000
retinitis pigmentosa 0.000
mercaptolactate-cysteine disulfiduria 0.000
Johanson-Blizzard syndrome 0.000
Smith-Fineman-Myers syndrome 0.000
monosomy 12p 0.000
Lennox-Gastaut syndrome 0.000
low IQ 0.000
dysplasia 0.000
hypomelanosis of Ito 0.000
brain atrophy 0.000
BBS3 0.000
intellectual impairment 0.000
onychodystrophy 0.000
Cockayne syndrome 0.000
Syndrome 0.000
Lennox-Gastaut syndrome 0.000
schizophrenia 0.000
psychosis 0.000
MRX23 0.000
Childhood psychosis 0.000
neurofaciodigitorenal syndrome 0.000
MCPH5 0.000
BDMR 0.000
hypertrichosis 0.000
Serum carnosinase deficiency 0.000
congenital disorder 0.000
Sex chromosome abnormalities 0.000
cardiofaciocutaneous syndrome 0.000
mental illness 0.000
megalocornea 0.000
monosomy 18p 0.000
bilateral cataracts 0.000
Jacobsen syndrome 0.000
Marshall-Smith syndrome 0.000
Cornelia de Lange 0.000
Lenz-Majewski syndrome 0.000
X-linked alpha-thalassemia/mental retardation syndrome 0.000
ring chromosome 20 0.000
stereotypies 0.000
Zimmermann-Laband syndrome 0.000
scoliosis 0.000
Mietens' syndrome 0.000
LGMD2K 0.000
Ruvalcaba syndrome 0.000
CAMR 0.000
SPG1 0.000
maple syrup urine disease 0.000
Hennekam syndrome 0.000
hypogonadotropic hypogonadism 0.000
trisomy 12p 0.000
Filippi syndrome 0.000
cognitive impairment 0.000
DiGeorge syndrome 0.000
mannosidosis 0.000
MRX73 0.000
dermotrichic syndrome 0.000
FXTAS 0.000
4p minus syndrome 0.000
AMMECR1 0.000
Urban syndrome 0.000
ring chromosome 7 syndrome 0.000
lalling 0.000
MRX81 0.000
Tyrosinemia I 0.000
Constitutional obesity 0.000
Malpuech syndrome 0.000
APMR1 0.000
MDC1B 0.000
MRX63 0.000
Porteous syndrome 0.000
Sleep starts 0.000
Proud syndrome 0.000
MRX84 0.000
macrocephaly-cutis marmorata telangiectatica congenita syndrome 0.000
partial trisomy 1p 0.000
MRT2A 0.000
Aseptic meningitis or meningoencephalitis 0.000
Other mental retardation 0.000
7p partial trisomy syndrome 0.000
Mollica-Pavone-Anterer syndrome 0.000
MRX14 0.000
Cranial nerve compression 0.000
MRXSL 0.000
Hall-Riggs syndrome 0.000
MRX59 0.000
Congenital dysphasia 0.000
FGS4 0.000
Disturbance of emotions specific to childhood and adolescence 0.000
MRXS7 0.000
MRX20 0.000
ATS-MR 0.000
MRX77 0.000
MRX52 0.000
muscular dystrophy 0.000
Klinefelter's syndrome 0.000
arachnodactyly 0.000
partial trisomy 19p 0.000
trisomy 10q 0.000
Hyperprolinemia type I 0.000
DM1 0.000
blindness 0.000
velocardiofacial syndrome 0.000
mucopolysaccharidosis 0.000
galactosemia 0.000
hyperprolinemia 0.000
Turner syndrome 0.000
sensorineural hearing loss 0.000
ring chromosome 15 syndrome 0.000
cleft lip/palate 0.000
prolapse 0.000
ADHD 0.000
Hopkins syndrome 0.000
LGS 0.000
13q deletion syndrome 0.000
myopathy 0.000
nystagmus 0.000
congenital infection 0.000
KBG syndrome 0.000
MPS VII 0.000
CBS deficiency 0.000
pseudopseudohypoparathyroidism 0.000
ACLS 0.000
Sanfilippo syndrome 0.000
hydroxyprolinemia 0.000
Michels syndrome 0.000
developmental aphasia 0.000
Peters-plus syndrome 0.000
tetrasomy 18p 0.000
trisomy 22 0.000
hyperornithinemia 0.000
Duchenne muscular dystrophy 0.000
tyrosinemia 0.000
monosomy 21 0.000
FRA11B 0.000
MDC1C 0.000
hemiparesis 0.000
Hawkinsinuria 0.000
partial trisomy 6q 0.000
obesity 0.000
Dubowitz 0.000
trisomy 9 0.000
Brachydactyly 0.000
brain dysfunction 0.000
language disorder 0.000
Congenital cerebellar ataxia 0.000
MRX82 0.000
Atypical absence seizures 0.000
Carnevale syndrome 0.000
Circumscribed storiform collagenoma 0.000
ring chromosome 12 0.000
MRX50 0.000
Linear nevus 0.000
Primary pulmonary TB 0.000
Pallidoluysian atrophy 0.000
Nodding spasm 0.000
FGS3 0.000
hypertelorism-hypospadias syndrome 0.000
Vasquez syndrome 0.000
Benign myoclonic epilepsy in infancy 0.000
MRX72 0.000
Non-bullous ichthyosiform erythroderma 0.000
Premature eruption of teeth 0.000
partial monosomy 2q 0.000
Phosphoglucomutase deficiency 0.000
Summitt syndrome 0.000
Brooks syndrome 0.000
Progressive cardiomyopathic lentiginosis 0.000
Mutchinick syndrome 0.000
Hamel syndrome 0.000
MRX58 0.000
Dihydrofolate reductase deficiency 0.000
Motor Skills Disorders 0.000
partial monosomy 9q 0.000
tyrosinuria 0.000
fits 0.000
Asperger syndrome 0.000
Lowe 0.000
CHARGE association 0.000
Drash syndrome 0.000
LIS1 0.000
attention-seeking 0.000
SPG15 0.000
alpha-Mannosidosis 0.000
Autistic behavior 0.000
incontinentia pigmenti 0.000
metabolic disorder 0.000
BBS6 0.000
attention deficit disorder 0.000
SPG11 0.000
MEHMO 0.000
NHBP 0.000
inverted duplication of chromosome 15 0.000
Primary congenital hypothyroidism 0.000
trisomy 8p 0.000
schizencephaly 0.000
heart disease 0.000
Hurler 0.000
DMC 0.000
trisomy 15q 0.000
specific developmental disorders 0.000
Wolcott-Rallison syndrome 0.000
Fukuyama congenital muscular dystrophy 0.000
aggression 0.000
growth hormone deficiency 0.000
CLN5 0.000
Kelley-Seegmiller syndrome 0.000
6p deletion syndrome 0.000
MKKS 0.000
ATMDS 0.000
Sanfilippo 0.000
partial trisomy 11q 0.000
Talkativeness 0.000
r(18) syndrome 0.000
Homozygous variegate porphyria 0.000
ENFL2 0.000
Gurrieri syndrome 0.000
SPG24 0.000
ring chromosome 13 syndrome 0.000
Hyperprolinemia type II 0.000
vLINCL 0.000
Odontogenic myxofibroma 0.000
developmental delay disorders 0.000
Familial mastocytosis 0.000
Neonatal intracranial hemorrhage 0.000
Nerve deafness 0.000
X-Linked Mental Retardation 0.000
Borjeson-Forssman-Lehmann syndrome 0.000
Molybdenum deficiency 0.000
Eastman-Bixler syndrome 0.000
Myhre syndrome 0.000
premature ovarian failure 0.000
mutism 0.000
Greig cephalopolysyndactyly syndrome 0.000
C syndrome 0.000
MCPH6 0.000
Sulfite oxidase deficiency 0.000
chondrodysplasia 0.000
dementia 0.000
TRPS1 0.000
hyperargininemia 0.000
Supravalvular aortic stenosis 0.000
OSX 0.000
Kenny-Caffey syndrome 0.000
Toriello-Carey syndrome 0.000
Cross syndrome 0.000
Behr syndrome 0.000
MICA 0.000
Crouzon syndrome 0.000
precocious puberty 0.000
trisomy 10p 0.000
RBS 0.000
DFN6 0.000
Laminar heterotopia 0.000
MCPH3 0.000
CAMOS 0.000
Hemiplegic cerebral palsy 0.000
Cobalamin C disease 0.000
Fontaine syndrome 0.000
catatonic psychosis 0.000
Pollitt syndrome 0.000
Thyroid hypoplasia 0.000
Precursor T-cell lymphoblastic lymphoma 0.000
ATLD 0.000
Amsterdam dwarfism 0.000
minimal brain dysfunction 0.000
Apert syndrome 0.000
trisomy 14 0.000
partial trisomy 16p 0.000
WHSCR 0.000
SPG21 0.000
Epidermal nevus syndrome 0.000
Trichorhinophalangeal syndrome 0.000
XXYY syndrome 0.000
DFN3 0.000
MPS II 0.000
osteodystrophy 0.000
neurological disease 0.000
apraxia 0.000
head-banging 0.000
myoclonus epilepsy 0.000
hypoparathyroidism 0.000
Congenital myotonic dystrophy 0.000
Simpson-Golabi-Behmel syndrome 0.000
Congenital muscular dystrophy 0.000
MPS I 0.000
Microdysgenesis 0.000
MCPH2 0.000
glycogen storage disease 0.000
pseudobulbar palsy 0.000
CCAL2 0.000
CMTX4 0.000
Congenital hyperthyroidism 0.000
Early onset cerebellar ataxia with retained tendon reflexes 0.000
Severe childhood autosomal recessive muscular dystrophy 0.000
Spastic ataxia 0.000
habitual drunkenness 0.000
ROCA 0.000
Marfanoid hypermobility syndrome 0.000
glutamate formiminotransferase deficiency 0.000
Esophageal atresia/tracheoesophageal fistula 0.000
SCAR8 0.000
goiter 0.000
congenital rubella 0.000
Adenylosuccinate lyase deficiency 0.000
hyperglycinemia 0.000
BPES 0.000
Waardenburg syndrome 0.000
cataract 0.000
SPG2 0.000
hypermethioninemia 0.000
dup(3q) syndrome 0.000
Osteopathia striata with cranial sclerosis 0.000
myopia 0.000
Congenital methemoglobinemia 0.000
trisomy 12q 0.000
temper tantrum 0.000
Spastic quadriplegia 0.000
sialidosis 0.000
ectodermal dysplasia 0.000
aortic stenosis 0.000
methylmalonic acidemia 0.000
MPS IIIA 0.000
neonatal asphyxia 0.000
renal tubular acidosis 0.000
EVR1 0.000
atonic seizure 0.000
partial trisomy 17q 0.000
recombinant 8 syndrome 0.000
sphingomyelinosis 0.000
Verbal dyspraxia 0.000
HSAN V 0.000
Multiple renal cysts 0.000
MRT1 0.000
methionine synthase deficiency 0.000
Mechanical intestinal obstruction 0.000
Early Onset Cerebellar Ataxia 0.000
Rhizomelic chondrodysplasia punctata 0.000
lysosomal storage disease 0.000
histidinemia 0.000
alcohol-related neurodevelopmental disorder 0.000
partial trisomy 4q 0.000
XYY syndrome 0.000
anal atresia 0.000
HND 0.000
X-linked hereditary disease 0.000
febrile convulsions 0.000
neurofibromatosis 0.000
NPHP1 0.000
disorders of amino acid metabolism 0.000
Alzheimer's disease 0.000
Facial angiofibromas 0.000
Proximal renal tubular acidosis 0.000
status epilepticus 0.000
echolalia 0.000
trisomy 8 0.000
benign neoplasm of the skin 0.000
Multiple carboxylase deficiency 0.000
Psychotic episodes 0.000
bacterial CNS infection 0.000
absence of status epilepticus 0.000
CIID 0.000
XK-aprosencephaly syndrome 0.000
CDG Ix 0.000
de Barsy syndrome 0.000
XLAG 0.000
SPG9 0.000
sialic acid storage disease 0.000
HHH 0.000
peripheral neuropathy 0.000
delayed puberty 0.000
trichorrhexis 0.000
BBS7 0.000
CLN7 0.000
muscular atrophy 0.000
hydrometrocolpos 0.000
Congenital fiber type disproportion 0.000
Succinic semialdehyde dehydrogenase deficiency 0.000
psychiatric diagnosis 0.000
Morquio 0.000
hypotrichosis 0.000
Periventricular leukomalacia 0.000
tetrasomy 9p 0.000
tyrosinosis 0.000
Proteus syndrome 0.000
SLS 0.000
LEOPARD syndrome 0.000
Salla disease 0.000
neurofibromatosis-Noonan syndrome 0.000
Fanconi syndrome 0.000
frotteurism 0.000
partial trisomy 14q 0.000
STS 0.000
speech disorder 0.000
HSAN 0.000
emotional disturbance 0.000
Giant axonal neuropathy 0.000
monosomy 7p 0.000
SPONASTRIME 0.000
Compensated hypothyroidism 0.000
Greenberg dysplasia 0.000
Atrophy of the corpus callosum 0.000
Gorlin-Chaudhry-Moss syndrome 0.000
spondyloperipheral dysplasia 0.000
complex partial seizures 0.000
Inborn errors of metabolism 0.000
gonadoblastoma 0.000
Canavan 0.000
Pfeiffer syndrome 0.000
BBS12 0.000
movement disorder 0.000
limb-girdle muscular dystrophy 0.000
Cardiac rhabdomyoma 0.000
LGMD2I 0.000
Hanhart 0.000
childhood schizophrenia 0.000
BMD 0.000
chorioretinitis 0.000
Colonic volvulus 0.000
partial trisomy 3p 0.000
Cowden syndrome 0.000
radioulnar synostosis 0.000
Speech impairment 0.000
acanthosis nigricans 0.000
congenital toxoplasmosis 0.000
Jordan's anomaly 0.000
trisomy 22q 0.000
DFN2 0.000
fibrocystic disease of the pancreas 0.000
Internal hydrocephalus 0.000
Mental and behavioral disorders 0.000
MDC1D 0.000
phakoma 0.000
CLN9 0.000
JMS 0.000
OFD1 0.000
Mulvihill-Smith syndrome 0.000
osteopetrosis 0.000
Fanconi 0.000
maternal alcoholism 0.000
exotropia 0.000
pica 0.000
hypertrophic cardiomyopathy 0.000
articulation disorder 0.000
Alternating hemiplegia of childhood 0.000
Beckwith-Wiedemann syndrome 0.000
cytomegalovirus 0.000
TCD 0.000
multiple nevi 0.000
Tourette syndrome 0.000
ventricular dilatation 0.000
RP11 0.000
bipolar disorder 0.000
SPG30 0.000
Organic acidemias 0.000
Warkany syndrome 0.000
Fumarase deficiency 0.000
Ulerythema ophryogenes 0.000
trisomy 19q 0.000
DHPR deficiency 0.000
CMTX5 0.000
trisomy 1q 0.000
BBS8 0.000
kernicterus 0.000
hereditary motor and sensory neuropathy 0.000
hyperkeratosis 0.000
neurofibromatosis type 1 0.000
fetal infection 0.000
GRTH 0.000
cystinuria 0.000
conotruncal anomaly face syndrome 0.000
keratosis 0.000
trisomy 8q 0.000
abdominal obstruction 0.000
Ohtahara syndrome 0.000
SHS 0.000
10q deletion syndrome 0.000
OPA2 0.000
SPG28 0.000
spastic palsy 0.000
partial monosomy 21q 0.000
Congenital nephrogenic diabetes insipidus 0.000
alalia 0.000
DEFECT 0.000
KCS2 0.000
oculocerebrofacial syndrome 0.000
CMT2C 0.000
Ritscher-Schinzel syndrome 0.000
benign familial macrocephaly 0.000
atrichia 0.000
ventricular septal defect 0.000
Menkes 0.000
atrial septal defect 0.000
hyperphagia 0.000
Argininosuccinic aciduria 0.000
trisomy X 0.000
partial trisomy 2p 0.000
malnutrition 0.000
glaucoma 0.000
fucosidosis 0.000
pulmonic stenosis 0.000
conduct disorder 0.000
FHM2 0.000
Idiopathic epilepsy 0.000
Basal ganglia calcification 0.000
Nicolaides-Baraitser syndrome 0.000
hamartoma 0.000
retinopathy 0.000
ASG 0.000
ACS1 0.000
5-Oxoprolinuria 0.000
DSCR 0.000
Marie's ataxia 0.000
Nevus depigmentosus 0.000
Pitt-Rogers-Danks syndrome 0.000
ter Haar syndrome 0.000
Gynandroblastoma 0.000
MPS IIIC 0.000
Galactosialidosis 0.000
blepharophimosis-ptosis-epicanthus inversus syndrome 0.000
photosensitivity 0.000
NBS 0.000
cognitive deficit 0.000
pseudoglioma 0.000
personality disorder 0.000
leukodystrophy 0.000
Huntington's disease 0.000
prematurity 0.000
depression 0.000
PKS 0.000
cardiomyopathy 0.000
skin pigmentation disorder 0.000
floppy baby syndrome 0.000
transcobalamin II deficiency 0.000
Jaffe-Campanacci syndrome 0.000
Pili torti 0.000
Atlantoaxial instability 0.000
premature aging 0.000
organic brain syndrome 0.000
Leukocyte adhesion deficiency 0.000
moyamoya 0.000
Endemic goiter 0.000
gonadal dysgenesis 0.000
behavior problem 0.000
brain disorder 0.000
lipomatosis 0.000
hemiplegic migraine 0.000
congenital aplastic anemia 0.000
Central hypothyroidism 0.000
Neonatal anoxia 0.000
LCA5 0.000
FRA16A 0.000
MRX34 0.000
Chorioretinopathy 0.000
Peripheral pulmonary artery stenosis 0.000
psychomotor epilepsy 0.000
pyromania 0.000
Gyrate atrophy 0.000
GALT 0.000
EXT2 0.000
hypohidrosis 0.000
Pelizaeus-Merzbacher disease 0.000
CLN3 0.000
mitochondrial disease 0.000
learning disorder 0.000
mole 0.000
Galloway-Mowat syndrome 0.000
ethanolism 0.000
infantilism 0.000
Perinatal brain damage 0.000
Earwax 0.000
Cutis marmorata 0.000
Supravalvar aortic stenosis 0.000
trisomy 17p 0.000
taurodontism 0.000
esotropia 0.000
trisomy 13 0.000
mitochondrial encephalomyopathy 0.000
dysphasia 0.000
Charcot-Marie-Tooth disease 0.000
methemoglobinemia 0.000
pseudopterygium 0.000
Fregoli syndrome 0.000
glycinuria 0.000
congenital neuromuscular disorder 0.000
partial trisomy 7q 0.000
PCWH 0.000
Scheie 0.000
CMD 0.000
primary amenorrhea 0.000
Cerebro-costo-mandibular syndrome 0.000
neonatal jaundice 0.000
MDS 0.000
CMD 0.000
alcoholism 0.000
xeroderma pigmentosum 0.000
osteopoikilosis 0.000
LINCL 0.000
Musicogenic epilepsy 0.000
NALD 0.000
MILS 0.000
Mevalonate kinase deficiency 0.000
SPG4 0.000
Hypothalamic hamartoma 0.000
Robin 0.000
conductive hearing loss 0.000
congenital deafness 0.000
AIC 0.000
Behavioral problems 0.000
behavior disorder 0.000
affective disorder 0.000
Hereditary spastic paraplegia 0.000
Cheilitis glandularis 0.000
Infantile malignant osteopetrosis 0.000
PCBD 0.000
WWS 0.000
RP13 0.000
HHNK 0.000
Delleman syndrome 0.000
Dysostosis 0.000
SPG20 0.000
angiomyolipoma 0.000
Cortical dysplasia 0.000
Floating-Harbor syndrome 0.000
Leigh syndrome 0.000
aminoaciduria 0.000
Recklinghausen 0.000
Subependymal giant cell astrocytoma 0.000
Glycerol kinase deficiency 0.000
abortion 0.000
fibromatosis 0.000
Transverse colon 0.000
Dysosteosclerosis 0.000
GPHN 0.000
necatoriasis 0.000
elective mutism 0.000
Recurrent otitis media 0.000
partial trisomy 7p 0.000
hypolipoproteinemia 0.000
X;autosome translocation 0.000
pyorrhea 0.000
Transverse colon 0.000
Retinal dystrophy 0.000
Congenital ichthyosiform erythroderma 0.000
CDPX1 0.000
developmental language disorder 0.000
acute alcoholism 0.000
lactic acidosis 0.000
enzyme deficiency 0.000
propionic acidemia 0.000
neurobehavioral problems 0.000
Peroxisomal disorders 0.000
chromosome disorder 0.000
ICD 0.000
Cerebellum 0.000
Weaver 0.000
galactosuria 0.000
Potter facies 0.000
partial trisomy 2q 0.000
CMT2D 0.000
RP23 0.000
hypoglycemia 0.000
LWS 0.000
hypobetalipoproteinemia 0.000
Multiple epiphyseal dysplasia 0.000
MWS 0.000
Fraser 0.000
PAPA 0.000
Epileptic encephalopathy 0.000
anarthria 0.000
MBS 0.000
Mucolipidosis type IV 0.000
Infantile neuronal ceroid lipofuscinosis 0.000
dyslexia 0.000
self-destructive behavior 0.000
neuropathy 0.000
West 0.000
endocrine disorder 0.000
aphasia 0.000
psychomotor impairment 0.000
Kallmann's syndrome 0.000
fructose-1,6-diphosphatase deficiency 0.000
Cotard's syndrome 0.000
lymphangioleiomyomatosis 0.000
Weber syndrome 0.000
substance abuse 0.000
Nonconvulsive status epilepticus 0.000
Pontocerebellar hypoplasia 0.000
goniodysgenesis 0.000
insanity 0.000
rare disease 0.000
GALK 0.000
MPS IIID 0.000
Opsoclonus myoclonus 0.000
trisomy 18q 0.000
Carbohydrate-deficient glycoprotein syndrome 0.000
chorioretinal atrophy 0.000
neuronal ceroid lipofuscinosis 0.000
aspiration pneumonia 0.000
Stereotypy 0.000
WSS 0.000
CLN1 0.000
nephrogenic diabetes insipidus 0.000
night blindness 0.000
hyperopia 0.000
citrullinemia 0.000
leukoencephalopathy 0.000
SACS 0.000
delayed language 0.000
recurrent cholecystitis 0.000
CLN10 0.000
Wildervanck syndrome 0.000
hyperuricemia 0.000
quadriparesis 0.000
hernia 0.000
external genitalia 0.000
hearing disability 0.000
rubella 0.000
peg-shaped teeth 0.000
SCA8 0.000
coma 0.000
Hallervorden-Spatz disease 0.000
Goldenhar syndrome 0.000
Refsum disease 0.000
delusions 0.000
Coats' disease 0.000
Congenital hepatic fibrosis 0.000
PME 0.000
KCS 0.000
keratosis 0.000
Pelger-Huet 0.000
Reye 0.000
SPG6 0.000
4q deletion syndrome 0.000
Primary hypogonadism 0.000
adjustment disorder 0.000
autonomic neuropathy 0.000
CHARGE syndrome 0.000
Axis I diagnosis 0.000
sensory neuropathy 0.000
DFNA5 0.000
dyskeratosis congenita 0.000
hereditary sensory neuropathy 0.000
Hypoxic-ischemic brain injury 0.000
Meadow 0.000
CMT2E 0.000
Fasting hypoglycemia 0.000
Chronic progressive external ophthalmoplegia 0.000
RHS 0.000
FGD1 0.000
paranoid schizophrenia 0.000
Edwards 0.000
DES 0.000
Neonatal hyperthyroidism 0.000
nonorganic psychosis 0.000
CLN6 0.000
cafe au lait spots 0.000
hypercalcemia 0.000
chronic brain syndrome 0.000
LAD2 0.000
osteochondrodysplasia 0.000
CLN2 0.000
HRD 0.000
SGS 0.000
mitochondrial myopathy 0.000
CTX 0.000
Disorder 0.000
Auditory processing disorder 0.000
necrophilia 0.000
Intractable epilepsy 0.000
dysbasia 0.000
Cystic disease 0.000
SPG31 0.000
JHS 0.000
Abnormal behavior 0.000
warfarin embryopathy 0.000
parkinsonism 0.000
emotional disorder 0.000
W syndrome 0.000
triplegia 0.000
BBS9 0.000
mole 0.000
Zellweger syndrome 0.000
cognitive disorder 0.000
PHS 0.000
inguinal hernia 0.000
NPHP2 0.000
Angular cheilitis 0.000
GM1 gangliosidosis 0.000
aerophagia 0.000
BGS 0.000
pediatric disorder 0.000
skin ulcers 0.000
lymphedema 0.000
astrocytoma 0.000
cerebellar syndrome 0.000
immune deficiency 0.000
MERRF 0.000
Batten 0.000
generalized seizure 0.000
Frohlich 0.000
hyperlysinemia 0.000
infantile paralysis 0.000
Feingold syndrome 0.000
TBCD 0.000
Bartter's syndrome 0.000
FMD 0.000
PNP deficiency 0.000
funnel chest 0.000
BBS10 0.000
cutaneous leiomyoma 0.000
Hypothalamic dysfunction 0.000
tardive dyskinesia 0.000
osteosclerosis 0.000
sleep disorders 0.000
polycystic kidney 0.000
HMSN II 0.000
Distemper 0.000
ARTS 0.000
toxoplasmosis 0.000
gastroesophageal reflux disease 0.000
Pelizaeus-Merzbacher 0.000
Other variants 0.000
gynecomastia 0.000
renal failure 0.000
Chondrodysplasia punctata 0.000
Mongolian spots 0.000
Klebsiella sepsis 0.000
MKS3 0.000
SCA5 0.000
Catastrophic Illness 0.000
Segmental demyelination 0.000
adrenal insufficiency 0.000
Friedreich's ataxia 0.000
schizophreniform psychosis 0.000
generalized lipodystrophy 0.000
Neonatal seizures 0.000
Miller syndrome 0.000
RTS 0.000
trisomy 2 0.000
MELAS 0.000
compulsion 0.000
Griscelli syndrome 0.000
retinopathy of prematurity 0.000
achalasia 0.000
hydronephrosis 0.000
Alstrom syndrome 0.000
Vogt 0.000
immaturity 0.000
hypochloremia 0.000
trichobezoar 0.000
esophoria 0.000
Alexander disease 0.000
intermittent explosive disorder 0.000
olivopontocerebellar atrophy 0.000
Molybdenum cofactor deficiency 0.000
panmyelosis 0.000
CPS deficiency 0.000
USH3 0.000
Ichthyosis vulgaris 0.000
Kearns-Sayre syndrome 0.000
obsessive-compulsive disorder 0.000
Hughes syndrome 0.000
gynecologic neoplasm 0.000
Optic disc drusen 0.000
Erythrokeratodermia variabilis 0.000
Communicating hydrocephalus 0.000
nevoid basal cell carcinoma syndrome 0.000
PDH deficiency 0.000
Infections of the central nervous system 0.000
hereditary ataxia 0.000
Darier's disease 0.000
infertility 0.000
septal defect 0.000
renal cyst 0.000
Alport syndrome 0.000
tonic-clonic status epilepticus 0.000
clotting factor deficiency 0.000
panhypopituitarism 0.000
XPD 0.000
TAR syndrome 0.000
CSB 0.000
Lennox syndrome 0.000
pancreatic insufficiency 0.000
neuromuscular disorder 0.000
Weill-Marchesani syndrome 0.000
CSB 0.000
dyskinesia 0.000
hypopituitarism 0.000
hearing disorder 0.000
dental caries 0.000
diabetes insipidus 0.000
familial disorder 0.000
female subfertility 0.000
homocystinemia 0.000
focal epilepsy 0.000
tumor 0.000
osteoporosis 0.000
sleep disturbances 0.000
Tag 0.000
residual schizophrenia 0.000
Axis II diagnosis 0.000
undifferentiated schizophrenia 0.000
MPS VI 0.000
Klippel-Trenaunay syndrome 0.000
folate deficiency 0.000
polyneuropathy 0.000
FDH 0.000
poliosis 0.000
transvestism 0.000
SRS 0.000
simple schizophrenia 0.000
arcus senilis 0.000
xanthomatosis 0.000
trichotillomania 0.000
angiokeratoma 0.000
alcohol abuse 0.000
Kufs' disease 0.000
oppositional defiant disorder 0.000
Congenital heart disease 0.000
Robinow syndrome 0.000
nephrocalcinosis 0.000
DFNB4 0.000
ASD II 0.000
ornithine transcarbamylase deficiency 0.000
choroid plexus papilloma 0.000
MELAS 0.000
Ondine's curse 0.000
Klippel 0.000
APC 0.000
communication disorder 0.000
insulin coma 0.000
myeloradiculitis 0.000
hemeralopia 0.000
adjustment reaction 0.000
hemangioma 0.000
Landau-Kleffner syndrome 0.000
Grisel's syndrome 0.000
duodenal polyp 0.000
serous otitis media 0.000
Ondine's curse 0.000
endocrine neoplasm 0.000
cancer 0.000
megaloblastic anemia 0.000
sexual abuse 0.000
Maladjustment 0.000
Marfan syndrome 0.000
Factor VII deficiency 0.000
VATER association 0.000
MRS 0.000
organic psychosis 0.000
spondyloepiphyseal dysplasia 0.000
Young's syndrome 0.000
XPB 0.000
grand mal epilepsy 0.000
Currarino triad 0.000
muscle neoplasm 0.000
anemia 0.000
orotic aciduria 0.000
Palmoplantar keratoderma 0.000
trisomy 15 0.000
OFC 0.000
staphyloma 0.000
neuroticism 0.000
steatocystoma multiplex 0.000
glutaric aciduria 0.000
Cardiac defects 0.000
TSH deficiency 0.000
SCS 0.000
hormone deficiency 0.000
NMS 0.000
RGS 0.000
DPD deficiency 0.000
hallucinations 0.000
hyperthyroidism 0.000
PHP 0.000
Epilepsia partialis continua 0.000
Rabson-Mendenhall syndrome 0.000
thumb-sucking 0.000
hyperhomocysteinemia 0.000
Intrauterine infection 0.000
Lhermitte-Duclos disease 0.000
megacolon 0.000
leprechaunism 0.000
anxious state 0.000
Central precocious puberty 0.000
Hemangioblastoma 0.000
CGL1 0.000
cystathioninuria 0.000
lens opacity 0.000
triploidy 0.000
Mendelian disorders 0.000
diabetes 0.000
sensory disturbance 0.000
mitral valve prolapse 0.000
schizoaffective disorder 0.000
anxiety disorders 0.000
Gingival hyperplasia 0.000
Odontogenic myxoma 0.000
High myopia 0.000
Generalized epilepsy 0.000
hematological abnormality 0.000
psycho-organic syndrome 0.000
craniofrontonasal syndrome 0.000
cherubism 0.000
mixed deafness 0.000
sideroblastic anemia 0.000
keratitis 0.000
Parkinson's disease 0.000
metachromatic leukodystrophy 0.000
WS4 0.000
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy 0.000
tic 0.000
hereditary chorea 0.000
Biotin deficiency 0.000
CINCA syndrome 0.000
macrocytic anemia 0.000
variegate porphyria 0.000
memory impairment 0.000
SME 0.000
radiation carcinogenesis 0.000
LCA 0.000
retinoblastoma 0.000
acanthocytosis 0.000
TD2 0.000
congenital anemia 0.000
sleep apnea 0.000
Niemann-Pick 0.000
GCE 0.000
Familial hemiplegic migraine 0.000
monosomy 22 0.000
yellow nail syndrome 0.000
volvulus 0.000
renal disease 0.000
oligodendroglioma 0.000
immunodeficiency 0.000
encephalitis 0.000
Taenia solium infection 0.000
onychogryphosis 0.000
mania 0.000
hemolytic anemia 0.000
FRA 0.000
organic disease 0.000
Kniest dysplasia 0.000
HHG 0.000
hyperostosis 0.000
pancytopenia 0.000
progressive muscular atrophy 0.000
GS1 0.000
Minamata disease 0.000
cervical spinal stenosis 0.000
early onset schizophrenia 0.000
Cerebellar atrophy 0.000
petit mal 0.000
Korsakoff's syndrome 0.000
chronic otitis externa 0.000
staghorn calculus 0.000
familial dysautonomia 0.000
BOR syndrome 0.000
esophageal atresia 0.000
AMD 0.000
Frontal lobe 0.000
epiphysiolysis 0.000
meningitis 0.000
wasting 0.000
CTLN2 0.000
Mohr 0.000
hypokalemic alkalosis 0.000
Gardner's syndrome 0.000
MDC1A 0.000
Pisa syndrome 0.000
Civatte 0.000
proptosis 0.000
USH1C 0.000
alcoholic dementia 0.000
HMSN I 0.000
confusion 0.000
Congenital central hypoventilation syndrome 0.000
poikiloderma 0.000
psychotic depression 0.000
astigmatism 0.000
Carnitine deficiency 0.000
pituitary dwarfism 0.000
Tauri 0.000
protanopia 0.000
Opsoclonus 0.000
Usher syndrome 0.000
Pulmonary lymphangioleiomyomatosis 0.000
Ullrich 0.000
GEFS+ 0.000
thrombocytopenia 0.000
reflex epilepsy 0.000
dysphagia 0.000
Alpers 0.000
Wolff-Parkinson-White syndrome 0.000
FHM 0.000
memory distortion 0.000
bronchorrhea 0.000
Becker's nevus 0.000
Copper deficiency 0.000
external ear 0.000
basal ganglia disease 0.000
TD1 0.000
erythroderma 0.000
ADD 0.000
PBT 0.000
Nystagmus 0.000
breast fibroadenoma 0.000
ATE 0.000
SPG7 0.000
KAR 0.000
FRDA 0.000
ATM 0.000
CBCL 0.000
Hypoxic-ischemic encephalopathy (HIE) 0.000
Pituitary gland 0.000
Symptom
hypotonia 0.004
seizures 0.002
ataxia 0.001
cerebellar ataxia 0.000
spasticity 0.000
prominent nose 0.000
dystonia 0.000
weakness 0.000
dysarthria 0.000
hemiplegia 0.000
myoclonus 0.000
tremor 0.000
Posturing 0.000
athetosis 0.000
ataxic gait 0.000
drooling 0.000
hepatosplenomegaly 0.000
paraparesis 0.000
Dysdiadochokinesis 0.000
intention tremor 0.000
hypertonia 0.000
delayed language development 0.000
Spastic hemiplegia 0.000
Respiratory abnormalities 0.000
Tandem gait 0.000
partial seizure 0.000
enuresis 0.000
constipation 0.000
hyperacusis 0.000
Hypersomnolence 0.000
photophobia 0.000
clumsiness 0.000
catatonia 0.000
paresis 0.000
chromosome marker 0.000
Synkinesis 0.000
abnormal breathing 0.000
anesthesia 0.000
chorea 0.000
chronic constipation 0.000
tonic-clonic seizure 0.000
lethargy 0.000
Physical findings 0.000
incoordination 0.000
pachyonychia 0.000
vomiting 0.000
localized erythema 0.000
ophthalmoplegia 0.000
agitation 0.000
tonic seizure 0.000
hepatomegaly 0.000
fasciculation 0.000
abnormal gait 0.000
polyuria 0.000
polydipsia 0.000
clonus 0.000
bedwetting 0.000
musculoskeletal disability 0.000
carpopedal spasm 0.000
monoplegia 0.000
Kernig's sign 0.000
Psychiatric symptoms 0.000
generalized erythema 0.000
pain 0.000
DNA marker 0.000
General symptoms 0.000
physical appearance 0.000
Bitot's spots 0.000
pallor 0.000
sleepiness 0.000
staggering gait 0.000
thinning 0.000
splenomegaly 0.000
anosmia 0.000
cyanosis 0.000
headache 0.000
Behavioral symptoms 0.000
situational stress 0.000
regurgitation 0.000
consciousness disturbance 0.000
sighing 0.000
clubbing 0.000
growing pains 0.000
Involuntary Movement 0.000
aphonia 0.000
hypersomnia 0.000
joint stiffness 0.000
diarrhea 0.000
astasia 0.000
facial droop 0.000
decreased appetite 0.000
vestibulitis 0.000
insomnia 0.000
respiratory distress 0.000
nocturnal polyuria 0.000
dry skin 0.000
Hudson 0.000
muscle rigidity 0.000
scaly skin 0.000
Spastic 0.000
adipsia 0.000
rectal pain 0.000
Extrapyramidal symptoms 0.000
tachypnea 0.000
livedo 0.000
pedal edema 0.000
disturbed balance 0.000
snoring 0.000
abdominal cramps 0.000
anal pain 0.000
breath holding 0.000
apathy 0.000
periorbital edema 0.000
torticollis 0.000
stridor 0.000
Gastrointestinal symptoms 0.000
myalgia 0.000
auditory hallucination 0.000
overweight 0.000
abdominal pain 0.000
masculinization 0.000
lassitude 0.000
visual hallucination 0.000
memory loss 0.000
forgetfulness 0.000
hypothermia 0.000
stigma 0.000
ENT 0.000
Sedation 0.000
testicular pain 0.000
flank pain 0.000
cachexia 0.000
hunger 0.000
prostration 0.000
loss of taste 0.000
abdominal fullness 0.000
neurological disability 0.000
belching 0.000
loss of balance 0.000
blepharospasm 0.000
Halo 0.000
emaciation 0.000
hoarseness 0.000
dizziness 0.000
HSA 0.000
stomach pain 0.000
hemoptysis 0.000
Catch 0.000
fever of unknown origin 0.000
hyperesthesia 0.000
Decreased activity 0.000
muscle stiffness 0.000
Anoxia 0.000
ketonuria 0.000
personality change 0.000
excessive sweating 0.000
hopelessness 0.000
vertigo 0.000
pleuritic chest pain 0.000
spasm 0.000
nasal discharge 0.000
neck stiffness 0.000
asthenia 0.000
dyspnea 0.000
despair 0.000
fatigue 0.000
neuralgia 0.000
analgesia 0.000
paresthesia 0.000
colic 0.000
hip pain 0.000
renal colic 0.000
anorexia 0.000
blurred vision 0.000
syncope 0.000
distraction 0.000
bradykinesia 0.000
eds 0.000
urinary frequency 0.000
arthralgia 0.000
acute stress 0.000
nausea 0.000
cough 0.000
dental pain 0.000
numbness 0.000
shortness of breath 0.000
bitter taste 0.000
erythema 0.000
nausea and vomiting 0.000
sciatica 0.000
menopausal symptoms 0.000
hypocapnia 0.000
alexithymia 0.000
neck pain 0.000
collapse 0.000
oliguria 0.000
hypercapnia 0.000
starvation 0.000
heartburn 0.000
tense 0.000
exhaustion 0.000
rhinorrhea 0.000
Wind 0.000
discomfort 0.000
tinnitus 0.000
acute abdomen 0.000
Ill 0.000
discomfort 0.000
functional recovery 0.000
acidity 0.000
chest pain 0.000
angina 0.000
back pain 0.000
Welt 0.000
Drug
Quetiapine hemifumarate 0.000
Zmax 0.000
Calcium hopantenate 0.000
Fosfluconazole 0.000
Galsulfase 0.000
Thyradin 0.000
AGG 0.000
CXN 0.000
Azithromycin 0.000
Idursulfase 0.000
Diastat 0.000
Stiripentol 0.000
DM1 0.000
Sodium valproate 0.000
Namenda 0.000
Dermatol 0.000
Collodion 0.000
Valganciclovir 0.000
Amlexanox 0.000
Zinc acetate 0.000
Ethanol 0.000
BH4 0.000
Galactose 0.000
Spectrum 0.000
Cobalamin 0.000
lysine 0.000
Tiopronin 0.000
CSF 0.000
Sonata 0.000
Phenytoin 0.000
Sodium benzoate 0.000
Vitamin B 0.000
Thioridazine 0.000
Spectrum 0.000
DMAA 0.000
OTC 0.000
CLS 0.000
Pyridoxal phosphate 0.000
Meconium 0.000
OTC 0.000
AVC 0.000
Vitamin B12 0.000
Atomoxetine 0.000
Singular 0.000
PTH 0.000
Frontal 0.000
Ammonium chloride 0.000
Asn 0.000
ABC 0.000
L-tyrosine 0.000
Depo-Provera 0.000
Palmitoyl 0.000
Isotretinoin 0.000
Adenosine deaminase 0.000
CPO 0.000
Senna 0.000
Copaxone 0.000
Senna 0.000
Growth hormone 0.000
Ganciclovir 0.000
Growth hormone 0.000
Piracetam 0.000
HPMPC 0.000
Retinoic Acid 0.000
Zonisamide 0.000
VCR 0.000
Doyle 0.000
pyridoxal phosphate 0.000
Botox 0.000
ENT 0.000
Aminoguanidine 0.000
Parkin 0.000
TTC 0.000
Parkin 0.000
Orphan 0.000
BTC 0.000
Tuberculin 0.000
Metrizamide 0.000
linolenate 0.000
BLM 0.000
CTA 0.000
Pilocarpine 0.000
ETS 0.000
PDL 0.000
lactose 0.000
MgSO4 0.000
Everolimus 0.000
Bayer 0.000
Camp 0.000
CPR 0.000
DMSA 0.000
Riboflavin 0.000
TEL 0.000
ADM 0.000
Rosiglitazone 0.000
Lipiodol 0.000
Leaf 0.000
NADH 0.000
SF6 0.000
DBS 0.000
Gabapentin 0.000
THF 0.000
CAM 0.000
Propofol 0.000
Mutagen 0.000
p75 0.000
Prednisone 0.000
Luteinizing 0.000
vitamin E 0.000
EPA 0.000
HCG 0.000
Alliance 0.000
Aloe 0.000
CoCl2 0.000
CoCl2 0.000
Fluconazole 0.000
Vitamin A 0.000
FAD 0.000
Vitamin K 0.000
Prednisolone 0.000
MRC 0.000
GEO 0.000
TAC 0.000
Simvastatin 0.000
Diurnal 0.000
MAP 0.000
PTC 0.000
Bevacizumab 0.000
Amiloride 0.000
Portal 0.000
ROC 0.000
ADR 0.000
-deoxyadenosine 0.000
EPI 0.000
Dakar 0.000
NAG 0.000
ACT 0.000
nitroglycerin 0.000
G418 0.000
Estrogens 0.000
Angiotensin II 0.000
Fragment 0.000
CDP 0.000
TAT 0.000
Clonidine 0.000
Histamine 0.000
Imatinib 0.000
CTX 0.000
CTX 0.000
Alanine 0.000
Vitamin E 0.000
Retinoic acid 0.000
caffeine 0.000
niacin 0.000
citric acid 0.000
Nephron 0.000
CTX 0.000
Adriamycin 0.000
Nephron 0.000
Cardiovasc 0.000
Gel 0.000
NH3 0.000
ampicillin 0.000
DNase I 0.000
ROS 0.000
Monit 0.000
ascorbate 0.000
IFN-gamma 0.000
Dial 0.000
Asthma 0.000
Enzyme
7-dehydrocholesterol reductase 0.000
prolidase 0.000
glycine amidinotransferase 0.000
aspartylglucosaminidase 0.000
guanidinoacetate methyltransferase 0.000
phenylalanine hydroxylase 0.000
cystathionine beta-synthase 0.000
EC 1.2.1.48 0.000
hypoxanthine-guanine phosphoribosyltransferase 0.000
spermine synthase 0.000
adenylosuccinate lyase 0.000
glycerol kinase 0.000
6-pyruvoyltetrahydropterin synthase 0.000
Lod 0.000
NADH-cytochrome b5 reductase 0.000
uridyltransferase 0.000
serum carnosinase 0.000
histone demethylase 0.000
succinic semialdehyde dehydrogenase 0.000
alpha-L-iduronidase 0.000
neurosin 0.000
aspartoacylase 0.000
inosine triphosphatase 0.000
CYP27A1 0.000
glutamate formiminotransferase 0.000
alpha-N-acetylglucosaminidase 0.000
biotinidase 0.000
dihydroxyacetone phosphate acyltransferase 0.000
CTD kinase 0.000
ornithine transcarbamylase 0.000
arylsulfatase 0.000
BCKDH 0.000
4-hydroxyphenylpyruvate dioxygenase 0.000
dihydropteridine reductase 0.000
sarcosine dehydrogenase 0.000
phosphomannomutase 0.000
iduronate-2-sulfatase 0.000
trans-2-enoyl-CoA reductase 0.000
phosphoinositide 5-phosphatase 0.000
sulfite oxidase 0.000
sulfite oxidase 0.000
AIR synthetase 0.000
phytanoyl-CoA hydroxylase 0.000
tyrosine aminotransferase 0.000
gamma-glutamyl phosphate reductase 0.000
dimethylglycine dehydrogenase 0.000
alpha-mannosidase 0.000
branched-chain alpha-keto acid dehydrogenase 0.000
creatine kinase 0.000
cystathionine gamma-synthase 0.000
galactose-1-phosphate uridylyltransferase 0.000
LIS 0.000
glucoamylase 0.000
dihydroxyacetone-phosphate acyltransferase 0.000
ribose-5-phosphate isomerase 0.000
PHD 0.000
site-1 protease 0.000
guanylate kinase 0.000
histidase 0.000
3-mercaptopyruvate sulfurtransferase 0.000
mitogen-activated protein kinase 0.000
N-acetylglucosaminyltransferase II 0.000
tripeptidyl peptidase 0.000
protein kinase 0.000
urocanase 0.000
sulfatase 0.000
diphosphomevalonate decarboxylase 0.000
proline oxidase 0.000
phosphoglycerate kinase 0.000
sialidase 0.000
proline dehydrogenase 0.000
protoporphyrinogen oxidase 0.000
ornithine aminotransferase 0.000
amylo-1,6-glucosidase 0.000
CLK1 0.000
KAR 0.000
thyroid peroxidase 0.000
ubiquitin-protein ligase 0.000
ERK 0.000
pyruvate dehydrogenase phosphatase 0.000
isocitrate dehydrogenase 0.000
mevalonate kinase 0.000
NAD+ oxidoreductase 0.000
demethylase 0.000
3-oxoacid CoA-transferase 0.000
arylsulfatase A 0.000
isocitrate dehydrogenase 0.000
mannanase 0.000
PRPP synthetase 0.000
methionine adenosyltransferase 0.000
esterase D 0.000
gamma-glutamyl kinase 0.000
ATPase 0.000
site-1 protease 0.000
pyrroline-5-carboxylate dehydrogenase 0.000
MEK 0.000
N-acetylglucosaminyltransferase 0.000
GABA transaminase 0.000
T-protein 0.000
methylenetetrahydrofolate reductase 0.000
methylenetetrahydrofolate reductase 0.000
xanthine dehydrogenase 0.000
neuraminidase 0.000
deoxyguanosine kinase 0.000
spermidine synthase 0.000
malonyl-CoA decarboxylase 0.000
propionyl-CoA carboxylase 0.000
propionyl-CoA carboxylase 0.000
betaine-homocysteine methyltransferase 0.000
GTP cyclohydrolase I 0.000
beta-hydroxybutyrate dehydrogenase 0.000
homocysteine methyltransferase 0.000
histone acetyltransferase 0.000
superoxide dismutase 0.000
NOS 0.000
argininosuccinate synthetase 0.000
choline acetyltransferase 0.000
RNA polymerase 0.000
methylmalonyl-CoA mutase 0.000
beta-glucuronidase 0.000
lysine acetyltransferase 0.000
argininosuccinate lyase 0.000
aldehyde oxidase 0.000
sepiapterin reductase 0.000
kynureninase 0.000
catalase 0.000
STR 0.000
tetanus neurotoxin 0.000
NPL 0.000
methionine synthase reductase 0.000
acyl-CoA synthetase 0.000
acyl carrier protein synthase 0.000
methionine synthase 0.000
acyl-CoA synthetase 0.000
poly(ADP-ribose) glycohydrolase 0.000
adenylosuccinate synthetase 0.000
GM3 synthase 0.000
glutaryl-CoA dehydrogenase 0.000
pyridoxal kinase 0.000
cysteine dioxygenase 0.000
methionine synthase 0.000
beta-galactosidase 0.000
biotin carboxylase 0.000
arginase 0.000
guanase 0.000
cystathionine gamma-lyase 0.000
pyruvate carboxylase 0.000
carbonic anhydrase 0.000
pantothenate kinase 0.000
CaMKII 0.000
glycine decarboxylase 0.000
aldehyde dehydrogenase 0.000
alcohol dehydrogenase 0.000
PAL 0.000
HDR 0.000
pyruvate dehydrogenase 0.000
nucleoside hydrolase 0.000
galactokinase 0.000
GRK5 0.000
cytochrome oxidase 0.000
complex I 0.000
3-hydroxyacyl-CoA dehydrogenase 0.000
3-hydroxyacyl-CoA dehydrogenase 0.000
glucose-6-phosphate dehydrogenase 0.000
kinesin 0.000
CPS 0.000
phosphoglycerate dehydrogenase 0.000
acetoacetyl-CoA thiolase 0.000
alpha-L-fucosidase 0.000
alkaline phosphatase 0.000
ceramidase 0.000
SST 0.000
separase 0.000
PAL 0.000
glutathione peroxidase 0.000
Lys4 0.000
proteasome 0.000
acyl-CoA dehydrogenase 0.000
PAH 0.000
glucocerebrosidase 0.000
TOR 0.000
PME 0.000
nucleotide pyrophosphatase 0.000
triphosphatase 0.000
pyruvate dehydrogenase 0.000
rhodopsin kinase 0.000
pyruvate dehydrogenase 0.000
phosphorylase kinase 0.000
nitrilase 0.000
calcineurin 0.000
phospholipase A1 0.000
aldehyde dehydrogenase 0.000
HCS 0.000
ceruloplasmin 0.000
galactocerebrosidase 0.000
4-epimerase 0.000
monoamine oxidase 0.000
calpain 3 0.000
Protein 2 0.000
tryptophan hydroxylase 0.000
choline kinase 0.000
DOPA decarboxylase 0.000
STK11 0.000
HMG-CoA synthase 0.000
glucosylceramide synthase 0.000
aldehyde dehydrogenase 0.000
aldehyde dehydrogenase 0.000
adenylate kinase 0.000
aldehyde dehydrogenase 0.000
citrate synthase 0.000
alpha-L-fucosidase 0.000
fumarase 0.000
matriptase 0.000
myosin ATPase 0.000
chondroitinase 0.000
alpha-L-fucosidase 0.000
luciferase 0.000
chaperonin 0.000
chondroitinase 0.000
dihydropyrimidine dehydrogenase 0.000
ADH 0.000
alpha-ketoglutarate dehydrogenase 0.000
CDH 0.000
carboxypeptidase Y 0.000
N-acetyltransferase 0.000
tyrosine hydroxylase 0.000
enolase 0.000
RNase P 0.000
histidine kinase 0.000
PGM 0.000
PKG 0.000
AMP-activated protein kinase 0.000
TPP 0.000
phosphoinositide 3-kinase 0.000
DAT 0.000
diaphorase 0.000
Mg2+-ATPase 0.000
cathepsin D 0.000
succinate dehydrogenase 0.000
MDP 0.000
glutathione synthetase 0.000
PDH 0.000
diaphorase 0.000
AMP deaminase 0.000
adenine phosphoribosyltransferase 0.000
glutamate dehydrogenase 0.000
glutamate dehydrogenase 0.000
E-2 0.000
glutamate dehydrogenase 0.000
insulin-degrading enzyme 0.000
tyrosinase 0.000
CEP 0.000
protein phosphatase 2A 0.000
glutamate synthase 0.000
transcriptase 0.000
glutamate synthase 0.000
fructose 1,6-bisphosphatase 0.000
acyl-CoA dehydrogenase 0.000
acetylcholinesterase 0.000
MDH 0.000
glutamate synthase 0.000
APC 0.000
dihydropyrimidine dehydrogenase 0.000
SPS 0.000
galactose oxidase 0.000
adenosine deaminase 0.000
adenosine deaminase 0.000
caspase-3 0.000
pyruvate decarboxylase 0.000
PRE 0.000
MDH 0.000
aldolase 0.000
reverse transcriptase 0.000
KAT 0.000
S-adenosylmethionine decarboxylase 0.000
hexosaminidase 0.000
caspase-7 0.000
p100 0.000
thymidylate synthase 0.000
caspase-7 0.000
delta-aminolevulinic acid dehydratase 0.000
BIS 0.000
phosphofructokinase 0.000
trypsin 0.000
PTPase 0.000
glutathione reductase 0.000
DNA polymerase 0.000
neuropathy target esterase 0.000
5alpha-reductase 0.000
5alpha-reductase 0.000
diamine oxidase 0.000
CEP 0.000
3-hydroxy-3-methylglutaryl-CoA reductase 0.000
ATP synthase 0.000
protein kinase C 0.000
phosphodiesterase 0.000
renin 0.000
MAP 0.000
uricase 0.000
DNA ligase 0.000
DNA ligase 0.000
focal adhesion kinase 0.000
IKK 0.000
phosphatidylinositol 3-kinase 0.000
DNA methyltransferase 0.000
tissue plasminogen activator 0.000
heparinase 0.000
glucokinase 0.000
pyruvate kinase 0.000
CPR 0.000
carboxylesterase 0.000
xanthine oxidase 0.000
dopamine beta-hydroxylase 0.000
phosphorylase 0.000
cholinesterase 0.000
purine nucleoside phosphorylase 0.000
farnesyltransferase 0.000
AST 0.000
endonuclease 0.000
hyaluronidase 0.000
Alternating 0.000
glyceraldehyde-3-phosphate dehydrogenase 0.000
PDE 0.000
alanine aminotransferase 0.000
PTA 0.000
phosphoglucose isomerase 0.000
alpha-galactosidase 0.000
NADPH-diaphorase 0.000
NO synthase 0.000
cathepsin G 0.000
lactate dehydrogenase 0.000
endoglycosidase H 0.000
PAM 0.000
alpha-glucosidase 0.000
TdT 0.000
glutaminase 0.000
cathepsin L 0.000
AMPK 0.000
RNase 0.000
malate dehydrogenase 0.000
lactase 0.000
glutamate decarboxylase 0.000
lipoxygenase 0.000
TAT 0.000
sucrase 0.000
CD10 0.000
RNase 0.000
peroxiredoxin 0.000
BMT 0.000
asparaginase 0.000
myosin light chain kinase 0.000
NQO1 0.000
AMPK 0.000
micrococcal nuclease 0.000
ribonucleotide reductase 0.000
ribonuclease 0.000
ribonuclease 0.000
ribonucleotide reductase 0.000
GSK 0.000
lipoprotein lipase 0.000
furin 0.000
acid phosphatase 0.000
peroxidase 0.000
UDP-glucuronosyltransferase 0.000
thromboplastin 0.000
aspartate aminotransferase 0.000
cdc2 0.000
nitrate reductase 0.000
nitrate reductase 0.000
nitrate reductase 0.000
nitrate reductase 0.000
nitrate reductase 0.000
phospholipase D 0.000
nitrate reductase 0.000
gamma-glutamyl transpeptidase 0.000
topoisomerase 0.000
neutrophil elastase 0.000
heme oxygenase 0.000
glyceraldehyde-3-phosphate dehydrogenase 0.000
glyceraldehyde-3-phosphate dehydrogenase 0.000
topoisomerase 0.000
CPT 0.000
hyaluronidase 0.000
lipase 0.000
glyceraldehyde-3-phosphate dehydrogenase 0.000
transglutaminase 0.000
MIP 0.000
invertase 0.000
NADPH oxidase 0.000
thrombin 0.000
glyceraldehyde-3-phosphate dehydrogenase 0.000
glutathione S-transferase 0.000
PARP 0.000
caspase-8 0.000
urease 0.000
urease 0.000
caspase-9 0.000
DNase 0.000
ACE 0.000
phospholipase C 0.000
guanylate cyclase 0.000
plasmin 0.000
elastase 0.000
NADPH oxidase 0.000
urokinase-type plasminogen activator 0.000
chymotrypsin 0.000
beta-lactamase 0.000
phospholipase A2 0.000
collagenase 0.000
adenylate cyclase 0.000
ACS 0.000
lysozyme 0.000
Compound
Retard 0.008
MCA 0.000
MCA 0.000
Microcephalin 0.000
Guanidinoacetic acid 0.000
DNA 0.000
L-2-Hydroxyglutaric acid 0.000
DMD 0.000
Butoctamide hydrogen succinate 0.000
Caprin 0.000
DHC 0.000
Clin 0.000
Phe 0.000
Dec 0.000
Creatine 0.000
Tuberin 0.000
His 0.000
DSM 0.000
3-Hydroxyglutaric acid 0.000
Phenylpyruvate 0.000
Hydantoin 0.000
X 34 0.000
S-sulfocysteine 0.000
glutamic gamma-semialdehyde 0.000
PAC 0.000
adenylosuccinate 0.000
iodine 0.000
3-methyl-2-oxopentanoate 0.000
Neuronal 0.000
glutamate 0.000
Phenylalanine 0.000
homocysteine 0.000
MAOA 0.000
D-Proline 0.000
Thyroid 0.000
TSH 0.000
hydroxyglutarate 0.000
Triparanol 0.000
Bufotenine 0.000
N-acetylaspartic acid 0.000
Vigabatrin 0.000
GTP 0.000
tyrosine 0.000
AMPA 0.000
Sudafed 0.000
diphenylarsinic acid 0.000
N-acetylaspartic acid 0.000
Methylmalonic acid 0.000
6-pyruvoyltetrahydropterin 0.000
alpha-hydroxyisovaleric acid 0.000
Homocarnosine 0.000
Sudafed 0.000
ethanol 0.000
Valproic acid 0.000
mercaptopyruvate 0.000
GABA 0.000
GABA 0.000
Risperidone 0.000
Levetiracetam 0.000
SAICAR 0.000
arginine 0.000
Methylazoxymethanol 0.000
N-acetylaspartate 0.000
Cystathionine 0.000
proline 0.000
Cystathionine 0.000
isoleucine 0.000
L-methylmalonyl-CoA 0.000
pyrroline-5-carboxylate 0.000
isoleucine 0.000
valine 0.000
Homogentisate 0.000
BMD 0.000
TSC 0.000
Galactose 0.000
methionine 0.000
MSTFA 0.000
CZP 0.000
folinic acid 0.000
Zinc acetate 0.000
DDMS 0.000
SHM 0.000
iduronate 0.000
GAP 0.000
MOPA 0.000
MOPA 0.000
Pyridoxine 0.000
serine 0.000
DMDP 0.000
Guo 0.000
Ile 0.000
Cobalamin 0.000
A 3 0.000
DPH 0.000
gamma-aminobutyric acid 0.000
calcium 0.000
ESE 0.000
DIT 0.000
betaine 0.000
KTS 0.000
BIF 0.000
hexadecanal 0.000
lysine 0.000
XTP 0.000
5-oxoproline 0.000
5-oxoproline 0.000
Molybdenum cofactor 0.000
A 99 0.000
NMDA 0.000
hexadecanal 0.000
L-carnitine 0.000
Cilag 0.000
leucine 0.000
DCH 0.000
MMU 0.000
5-oxoproline 0.000
Guo 0.000
GDP-L-fucose 0.000
4-oxobutanoic acid 0.000
Xamoterol 0.000
Chlorpropamide 0.000
erythrose-4-phosphate 0.000
CH3-THF 0.000
ornithine 0.000
ornithine 0.000
ornithine 0.000
ornithine 0.000
ornithine 0.000
galactose 0.000
TNA 0.000
4-hydroxyphenylpyruvate 0.000
Cereb 0.000
SP 1 0.000
CLS 0.000
phosphocreatine 0.000
zinc 0.000
Pantothenate 0.000
Lamotrigine 0.000
3,4-dihydroxybenzaldehyde 0.000
docosanoic acid 0.000
Cyanidin 0.000
Harmine 0.000
5-oxoproline 0.000
IMP 0.000
urea 0.000
glutamine 0.000
creatinine 0.000
oxygen 0.000
corrin 0.000
Sulfatide 0.000
threonine 0.000
LTD 0.000
Spiramycin 0.000
GM2 0.000
AY9944 0.000
POP 0.000
Felbamate 0.000
Homocysteine 0.000
Homocysteine 0.000
Spiramycin 0.000
GML 0.000
2-Oxoglutarate 0.000
glucose 0.000
coenzyme Q10 0.000
Clobazam 0.000
Pac 0.000
Topiramate 0.000
Dolichol 0.000
Ibogaine 0.000
glutaryl-CoA 0.000
DBC 0.000
CoA 0.000
decarboxylated S-adenosylmethionine 0.000
Fenfluramine 0.000
3,4-dihydroxybenzaldehyde 0.000
Tetrahydrobiopterin 0.000
sulfate 0.000
Tiagabine 0.000
5-HIAA 0.000
asparagine 0.000
CHM 0.000
Thyroxine 0.000
Histoacryl 0.000
Hypoxanthine 0.000
tryptophan 0.000
ammonia 0.000
tryptophan 0.000
COS 0.000
Clomipramine 0.000
KIV 0.000
D-allose 0.000
ACTH 0.000
GM3 0.000
tryptophan 0.000
tryptophan 0.000
potassium 0.000
UDP-N-acetylgalactosamine 0.000
acetoacetyl-CoA 0.000
Ornithine 0.000
HBB 0.000
N-Acetylglucosamine 0.000
Clozapine 0.000
GAL 0.000
pentanedioic acid 0.000
water 0.000
Oxcarbazepine 0.000
cysteine 0.000
GDP 0.000
5-hydroxytryptophan 0.000
Vitamin D3 0.000
Aspartame 0.000
LCR 0.000
Mercury, 0.000
Mercury, 0.000
Mercury, 0.000
Mercury, 0.000
dihydrolipoamide 0.000
Mercury, 0.000
Mercury, 0.000
Proline 0.000
Mercury, 0.000
Zonisamide 0.000
aspartic acid 0.000
alanine 0.000
mercury 0.000
10-formyltetrahydrofolate 0.000
NDS 0.000
Pancuronium 0.000
barium 0.000
Isoproterenol 0.000
phosphate 0.000
Sarcosine 0.000
MEK 0.000
OCDD 0.000
neopterin 0.000
DES 0.000
CBS 0.000
ASN 0.000
Valine 0.000
adenosylmethionine 0.000
ATP 0.000
Sudan I 0.000
Levan 0.000
sodium 0.000
SET 0.000
PAS 0.000
Naltrexone 0.000
Cyproterone acetate 0.000
GMP 0.000
Valproic acid 0.000
cAMP 0.000
aspartic acid 0.000
trimethyllysine 0.000
Estrogen 0.000
pentanoic acid 0.000
HVA 0.000
Lead 0.000
O-acetylserine 0.000
salt 0.000
Carnitine 0.000
PYR 0.000
aspartic acid 0.000
Lithium 0.000
Taurocholate 0.000
PGA 0.000
aspartic acid 0.000
methylguanosine 0.000
Coenzyme Q10 0.000
iron 0.000
gamma-hydroxybutyric acid 0.000
CIT 0.000
AIB 0.000
copper 0.000
DHPG 0.000
PRN 0.000
40S 0.000
Succinylcholine 0.000
Asp 0.000
O-acetylserine 0.000
Alba 0.000
A 42 0.000
Cholesterol 0.000
Etretinate 0.000
TDT 0.000
PTS 0.000
Methimazole 0.000
Fluvoxamine 0.000
AMP 0.000
dGTP 0.000
Pimozide 0.000
6-12 0.000
DPC 0.000
DPC 0.000
DHB 0.000
FUDR 0.000
Methylphenidate 0.000
2-oxoglutarate 0.000
butyryl-CoA 0.000
PAH 0.000
DAMP 0.000
GD3 0.000
NMA 0.000
Fucose 0.000
DEK 0.000
EPSP 0.000
L-leucine 0.000
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