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

Human Gene/Protein
THG1L	12.0
C19orf2	11.5
PR domain containing 8	11.5
SANDO	11.3
KIAA0226	11.0
diacylglycerol kinase kappa	10.7
STM7	10.5
Troyer syndrome	10.5
PAPOLG	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

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
Facial lymphedema	12.0
childhood cerebellar astrocytoma	12.0
Familial visceral neuropathy	12.0
Dysfluency	11.7
SCA20	11.7
SCA25	11.7
SAX1	11.7
Dysprosody	11.7
SCA23	11.6
Hypokinetic dysarthria	11.6
Peripheral sensorimotor neuropathy	11.5
SPOAN	11.5
SCA4	11.5
Neuro-Behcet disease	11.5

Symptom
dysarthria	13.0
Gait deviation	13.0
Scanning speech	13.0
Frozen gait	11.5
Facial grimacing	11.5
Limb ataxia	11.5
left carotid bruit	11.0
Truncal ataxia	10.7
Paroxysmal dystonia	10.7
localized weakness	10.7
Sensory ataxia	10.5
poor balance and coordination	10.5
Premature loss of teeth	10.5
Retropulsion	10.3
Vertigo/dizziness	10.2
Ophthalmoparesis	10.2
quadrant anopsia	10.2
External ophthalmoplegia	10.2
Ataxic	10.2
Transient neurological symptoms	10.0

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