UMLS:C0013362 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0013362 (dysarthria)
3,768 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

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Human Gene/Protein
THG1L	12.0
PR domain containing 8	11.5
C19orf2	11.5
SANDO	11.3
KIAA0226	11.0
diacylglycerol kinase kappa	10.7
PAPOLG	10.5
STM7	10.5
Troyer syndrome	10.5
Hallervorden-Spatz syndrome	10.3
puratrophin-1	10.3
ANKFY1	10.2
anoctamin 10	10.2
SCA5	10.1
PANK2	10.1
PRDM8	10.0
SPG20	9.9
KIAA1840	9.9
ZNF407	9.9
junctional adhesion molecule 2	9.9
C19orf12	9.8
ARSACS	9.8
phosphodiesterase 8B	9.7
AARS2	9.7
glutaryl CoA dehydrogenase	9.7
spartin	9.7
LRP12	9.7
FAM36A	9.7
PKAN	9.6
UBQLN4	9.6
G protein-regulated inducer of neurite outgrowth 1	9.6
CSRP1	9.6
CMTX5	9.6
ZFYVE26	9.5
SCA11	9.5
KIAA1202	9.5
RCAN2	9.5
SPG15	9.4
KCNC3	9.4
SLC25A32	9.3

Disease
Dysarthria-clumsy hand syndrome	13.0
Spina bifida with hydrocephalus	13.0
Motor speech disorder	13.0
Fitzsimmons syndrome	13.0
palatoplegia	12.5
Ataxic dysarthria	12.3
Familial visceral neuropathy	12.0
Facial lymphedema	12.0
childhood cerebellar astrocytoma	12.0
SCA25	11.7
Dysprosody	11.7
Dysfluency	11.7
SAX1	11.7
SCA20	11.7
Hypokinetic dysarthria	11.6
SCA23	11.6
SCA4	11.5
Peripheral sensorimotor neuropathy	11.5
Neuro-Behcet disease	11.5
SPOAN	11.5
SANDO	11.3
Apraxia of speech	11.2
CAMOS	11.0
SCA18	11.0
Progressing stroke	11.0
Progressive cerebellar ataxia	11.0
SCA26	11.0
Bulbar weakness	11.0
Worster-Drought syndrome	11.0
Paraneoplastic cerebellar degeneration	10.9
Hypoglossal nerve palsy	10.9
glossoplegia	10.7
SCA13	10.7
Central alveolar hypoventilation syndrome	10.7
Migraine variants	10.7
Olivary hypertrophy	10.7
SCA5	10.7
torsion spasm	10.7
Behr syndrome	10.6
anarthria	10.5

Symptom
Gait deviation	13.0
dysarthria	13.0
Scanning speech	13.0
Frozen gait	11.5
Limb ataxia	11.5
Facial grimacing	11.5
left carotid bruit	11.0
Truncal ataxia	10.7
localized weakness	10.7
Paroxysmal dystonia	10.7
Sensory ataxia	10.5
Premature loss of teeth	10.5
poor balance and coordination	10.5
Retropulsion	10.3
Ophthalmoparesis	10.2
External ophthalmoplegia	10.2
Ataxic	10.2
Vertigo/dizziness	10.2
quadrant anopsia	10.2
hemiparesthesia	10.0
Transient neurological symptoms	10.0
facial droop	10.0
ataxic gait	9.8
Tandem gait	9.7
clumsiness	9.5
dyslalia	9.5
Pyramidal signs	9.5
hemihypesthesia	9.4
Kayser-Fleischer ring	9.4
intention tremor	9.3
amimia	9.1
arm weakness	9.1
cerebellar ataxia	9.1
disturbed speech	9.0
Flaccid paralysis	8.9
disturbance of sensation	8.9
ataxia	8.9
staggering gait	8.5
drooling	8.4
Aphasic	8.3

Enzyme
3-hydroxy-2-methylbutyryl-CoA dehydrogenase	11.5
pantothenate kinase	8.8
m-AAA protease	7.5
C1 esterase	7.0
deoxyguanosine kinase	6.9
phosphomannomutase	6.2
TSR	5.5
Lod	5.4
ceruloplasmin	5.4
thymidine phosphorylase	5.4
arylsulfatase A	4.8
CPM	4.7
phenylalanyl-tRNA synthetase	4.6
PME	4.5
alpha-L-iduronidase	4.5
biotinidase	4.4
succinyl-CoA synthetase	4.4
hexosaminidase	4.2
glucosylceramide synthase	4.1
tissue plasminogen activator	4.0
CYP27A1	4.0
CCS	3.8
thyroid peroxidase	3.8
PDH	3.6
GCA	3.6
methylenetetrahydrofolate reductase	3.6
methylenetetrahydrofolate reductase	3.6
NADH dehydrogenase	3.6
Alternating	3.4
acyl-CoA dehydrogenase	3.4
aconitase	3.3
acyl-CoA oxidase	3.1
SCS	3.1
creatine kinase	3.0
complex I	2.9
arylsulfatase	2.8
hypoxanthine-guanine phosphoribosyltransferase	2.7
BMT	2.7
sialidase	2.6
acyl-CoA dehydrogenase	2.6