UMLS:C0002986 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0002986 (Fabry)
5,646 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

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Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .

Human Gene/Protein
alpha-galactosidase A	0.083
alpha-galactosidase	0.022
GLA	0.007
X-linked	0.004
X-linked recessive	0.001
Gal	0.001
alpha-N-acetylgalactosaminidase	0.001
Gb3 synthase	0.000
alpha-GalA	0.000
NAGA	0.000
MPS II	0.000
GAL	0.000
glucosylceramide synthase	0.000
TINAGL1	0.000
ESX	0.000
A4GALT	0.000
FUCA1	0.000
MPS VI	0.000
PO42	0.000
alpha-L-fucosidase	0.000
glucocerebrosidase	0.000
Nance-Horan syndrome	0.000
MSPS	0.000
PBF	0.000
vascular endothelium	0.000
PRKAG2	0.000
aspartylglucosaminidase	0.000
Alport syndrome	0.000
forkhead box C1	0.000
CADASIL	0.000
Thrombospondin 2	0.000
SMF	0.000
ADAMTS6	0.000
COL4A1	0.000
SMSr	0.000
Chloride intracellular channel protein 1	0.000
PIP5K3	0.000
MPS2	0.000
aspartylglycosaminuria	0.000
allele b	0.000

Disease
Fabry	1.000
angiokeratoma	0.008
acroparesthesia	0.006
lysosomal storage disease	0.003
hypohidrosis	0.003
Gaucher disease	0.001
fucosidosis	0.001
Cornea verticillata	0.001
AMD	0.001
ventricular hypertrophy	0.000
MPS I	0.000
Niemann-Pick	0.000
Schindler disease	0.000
Krabbe disease	0.000
sphingolipidosis	0.000
proteinuria	0.000
hypertrophic cardiomyopathy	0.000
Fordyce	0.000
gangliosidosis	0.000
enzyme deficiency	0.000
Angiokeratoma of Fordyce	0.000
Storage disease	0.000
MPS II	0.000
metachromatic leukodystrophy	0.000
anhidrosis	0.000
Hurler	0.000
X-linked hereditary disease	0.000
Danon disease	0.000
mucopolysaccharidosis	0.000
Tay-Sachs disease	0.000
cystinosis	0.000
cardiomyopathy	0.000
Sandhoff disease	0.000
MPS VI	0.000
renal failure	0.000
erosio interdigitalis blastomycetica	0.000
chylomicron retention disease	0.000
Disorders of mitochondrial metabolism	0.000
GM1 gangliosidosis	0.000
Generalized hyperhidrosis	0.000

Symptom
Excruciating pain	0.000
Gastrointestinal signs and symptoms	0.000
Unexplained abdominal pain	0.000
sense loss	0.000
neurological pain	0.000
Stable angina pectoris	0.000
Burning pain	0.000
pain	0.000
Gastrointestinal symptoms	0.000
growing pains	0.000
Skin symptoms	0.000
paresthesia	0.000
Musculoskeletal symptoms	0.000
limb pain	0.000
bewilderment	0.000
rigors	0.000
Burning	0.000
tinnitus	0.000
exertional chest pain	0.000
abdominal pain	0.000
vertigo	0.000
generalized pain	0.000
hand pain	0.000
livedo	0.000
fever of unknown origin	0.000
arthralgia	0.000
atypical chest pain	0.000
Psychiatric symptoms	0.000
exertional angina	0.000
Physical findings	0.000
diarrhea	0.000
Neuropathic pain	0.000
dizziness	0.000
syncope	0.000
eds	0.000
dyspnea	0.000
numbness	0.000
excessive sweating	0.000
acute pain	0.000
Wind	0.000

Enzyme
alpha-galactosidase	0.052
ceramide trihexosidase	0.001
alpha-N-acetylgalactosaminidase	0.000
glucosylceramide synthase	0.000
glucocerebrosidase	0.000
aspartylglucosaminidase	0.000
alpha-L-fucosidase	0.000
N-acetylgalactosaminidase	0.000
alpha-L-fucosidase	0.000
alpha-L-fucosidase	0.000
FTR	0.000
cathepsin F	0.000
galactocerebrosidase	0.000
SOI	0.000
ACS	0.000
alpha-N-acetylglucosaminidase	0.000
hexosaminidase	0.000
arabinosidase	0.000
alpha-mannosidase	0.000
beta-glucosidase	0.000
NPL	0.000
beta-glucosidase	0.000
beta-galactosidase	0.000
iduronate-2-sulfatase	0.000
HK2	0.000
CDH	0.000
sulfatase	0.000
alpha-glucosidase	0.000
arylsulfatase A	0.000
PAM	0.000
adenine phosphoribosyltransferase	0.000
ascorbate oxidase	0.000
FPS	0.000
alpha-L-iduronidase	0.000
PMT	0.000
mannanase	0.000
prolidase	0.000
21-hydroxylase	0.000
lecithin:cholesterol acyltransferase	0.000
aromatic L-amino acid decarboxylase	0.000