UMLS:C0003635 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0003635 (apraxia)
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Human Gene/Protein
FAM149B1	13.5
C4orf21	13.5
senataxin	12.7
aprataxin	12.6
ALS4	12.5
ANKRD12	12.5
APTX	12.4
SETX	12.0
ZNF280D	11.9
MKS6	11.5
PNKP	11.4
ATLD	11.1
NAGPA	11.1
KPTN	10.9
PAPOLG	10.9
EFCAB4B	10.7
PIK3R5	10.7
FOXP2	10.6
TSPAN9	10.5
PARP11	10.5
IOSCA	10.5
SCAR1	10.3
nephrocystin-4	10.3
forkhead box P2	10.2
glutaryl CoA dehydrogenase	10.1
SANDO	10.1
FOXP2 protein	10.0
GLP2R	10.0
TMEM216	10.0
CDH18	10.0
cerebellin 1 precursor	10.0
POLG protein	9.9
Caytaxin	9.9
RIMS1	9.8
GATAD2B	9.8
NPHP1	9.7
NPHP4	9.6
B3GALNT2	9.6
AOA	9.6
nephrocystin	9.5
SLC30A9	9.5
CC2D2A	9.4
NGL-1	9.4
GNPTG	9.4
ZFHX4	9.3
MYO10	9.3
ADCK4	9.2
STX6	9.2
COQ4	9.2
Abelson helper integration site 1	9.0
PDE6D	9.0
COQ6	9.0
INPP5E	9.0
LBX1	8.9
thioesterase superfamily member 2	8.9
SMCR8	8.9
Disrupted in schizophrenia 1	8.9
PDSS2	8.8
TTRAP	8.8
NEK8	8.8
contactin 4	8.7
Synaptojanin 1	8.7
forkhead box P1	8.7
XRCC1 protein	8.6
SACS	8.6
SPTBN2	8.6
2E4	8.6
AHI1	8.6
TNRC6B	8.6
ADCK3	8.6
IMMP2L	8.6
GRID2	8.5
meiotic recombination 11	8.5
X-ray repair cross-complementing protein 1	8.5
ELP4	8.5
CNTNAP2	8.5
COQ9	8.5
GNPTAB	8.4
ATP8A2	8.4
ZNF423	8.4

Disease
Gestural apraxia	13.5
pathological emotionality	13.5
cortex; degeneration	13.5
Pallidonigral degeneration	13.5
apraxia	13.5
Presenile and senile dementia	13.5
Handwringing	13.5
Motor speech disorder	13.5
Ideational apraxia	13.2
Constructional apraxia	13.0
Ideomotor apraxia	13.0
Verbal dyspraxia	12.9
Oral apraxia	12.9
AOA2	12.6
cerebellotrigeminal and focal dermal dysplasia	12.5
Progressive Nonfluent Aphasia	12.5
Transcortical motor aphasia	12.5
Musical alexia	12.5
GD III	12.5
aphemia	12.3
Apraxia of speech	12.2
Corticobasal degeneration	12.2
Dysprosody	12.1
Logorrhea	11.9
ALS4	11.8
acalculia	11.8
ATLD	11.5
SCAE	11.5
Apraxia of gait	11.5
astereognosis	11.4
agraphia	11.3
CMT2B2	11.3
cognitive motor disorder	11.3
Delayed visual maturation	11.1
Spastic ataxia	11.1
Finger agnosia	11.1
Balint's syndrome	11.1
transcortical aphasia	11.0
agnosia	11.0
Early Onset Cerebellar Ataxia	10.9
autotopagnosia	10.9
moria	10.9
IOSCA	10.7
XLAG	10.7
anarthria	10.6
Cogan	10.6
speech disorder	10.5
articulation disorder	10.3
disturbed concentration	10.3
agrammatism	10.2
SANDO	10.1
writing disorder	10.1
anomia	10.1
alexia	10.0
Auditory agnosia	10.0
conduction aphasia	10.0
anosognosia	9.8
Joubert syndrome	9.8
dysgraphia	9.8
Pick's disease with Pick bodies	9.8
mild memory disturbance	9.8
ATP synthase deficiency	9.8
Wernicke's aphasia	9.7
aphasia	9.7
dyscalculia	9.7
word deafness	9.7
Adenylosuccinate lyase deficiency	9.7
NPHP4	9.6
motor aphasia	9.6
AOA	9.6
Idiopathic thrombocytopenia	9.5
SCAN1	9.4
MILS	9.4
Visual agnosia	9.4
Worster-Drought syndrome	9.4
WWS	9.3
Gillespie syndrome	9.2
Parietal lobe	9.2
language disorder	9.2
camptocormia	9.2

Symptom
Poverty of facial expression	13.5
Apraxic	13.0
Frozen gait	11.9
Extrapyramidal rigidity	11.9
amimia	10.6
Pyramidal signs	10.5
Respiratory abnormalities	10.1
clumsiness	9.9
Retropulsion	9.8
aprosodia	9.7
hemihypesthesia	9.4
blepharospasm	9.1
Bell's phenomenon	9.1
mirror writing	8.8
dysarthria	8.8
delayed language development	8.6
Aphasic	8.3
cerebellar ataxia	8.1
astasia	8.1
visual hallucination	8.1
Motor dysfunction	8.1
ataxia	8.1
personality change	7.9
myoclonus	7.9
Swallowing problems	7.9
Kernig's sign	7.9
Plantar flexion	7.9
bradykinesia	7.7
forgetfulness	7.6
General symptoms	7.6
dystonia	7.6
Opposition	7.4
asterixis	7.3
chorea	7.2
abiotrophy	7.1
Behavioral symptoms	7.1
aphonia	7.1
prominent nose	7.1
Parkinsonian tremor	7.1
athetosis	7.0
ataxic gait	6.9
Extrapyramidal symptoms	6.9
hypotonia	6.8
monoplegia	6.7
drooling	6.7
abnormal gait	6.6
Visual disturbances	6.6
apathy	6.5
hemiplegia	6.5
memory loss	6.5
muscle rigidity	6.4
incoordination	6.4
paresis	6.2
Neurologic symptoms	5.9
arm weakness	5.9
ophthalmoplegia	5.7
spasticity	5.6
tremor	5.6
metamorphopsia	5.5
hypertonia	5.5
tonic-clonic seizure	5.4
Psychiatric symptoms	5.1
clonus	4.9
prostration	4.9
loss of taste	4.9
Involuntary Movement	4.8
motor symptom	4.6
weakness	4.5
hyperemesis gravidarum	4.4
paraparesis	4.4
ketonuria	4.4
breath holding	4.3
limb pain	4.1
leg edema	4.1
partial seizure	4.0
CSR	4.0
agitation	4.0
hepatosplenomegaly	3.9
seizures	3.9
anosmia	3.9

Enzyme
m-AAA protease	7.9
TUT	7.8
polynucleotide kinase	7.1
3'-phosphatase	7.1
galactose-1-phosphate uridylyltransferase	6.7
GalT	6.3
sepiapterin reductase	5.9
adenylosuccinate lyase	5.9
Lod	5.9
uridyltransferase	5.7
glucocerebrosidase	5.5
FAST	4.9
CYP27A1	4.4
galactokinase	4.2
GTP cyclohydrolase I	4.1
NAT	4.1
RNA ligase	4.1
DNA ligase	4.0
DNA ligase	4.0
GCA	4.0
acyl-CoA dehydrogenase	3.8
GABA transaminase	3.8
LasR	3.7
botulinum neurotoxin	3.6
SCS	3.5
phenylalanine hydroxylase	3.0
acyl-CoA dehydrogenase	3.0
DAT	2.9
TOR	2.9
ornithine transcarbamylase	2.7
choline acetyltransferase	2.4
cholinesterase	2.4
NADH dehydrogenase	2.4
STR	1.8
DNA polymerase	1.7
PARP	1.7
phosphatidylinositol 3-kinase	1.6
enolase	1.6
acetylcholinesterase	1.5
citrate synthase	1.3
MIP	1.2
RNA polymerase	1.2
ceruloplasmin	1.2
urokinase-type plasminogen activator	1.1
phosphorylase	1.0
diaphorase	0.9
creatine kinase	0.8
aldehyde dehydrogenase	0.8
GSK	0.7
cytochrome oxidase	0.4
complex I	0.3
topoisomerase	0.3
phosphodiesterase	0.3
topoisomerase	0.2
catalase	0.0
tissue plasminogen activator	-0.0
thromboplastin	-0.2
tyrosine hydroxylase	-0.4
protein kinase	-0.5
RNase	-0.5
RNase	-0.7
luciferase	-0.8
proteasome	-1.3
lactate dehydrogenase	-1.4
thrombin	-1.6
alkaline phosphatase	-2.1
mitogen-activated protein kinase	-3.1