UMLS:C0153640 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0153640 (Cerebellum)
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Human Gene/Protein
SYNE1 protein	14.1
KIAA0960	14.1
CAPS2 protein	13.1
zinc finger protein 4	13.1
ITPR1 protein	12.5
Thg-1pit	12.5
KIAA0226	12.1
SCA10	11.5
FERD3L	11.5
EEFSEC	11.3
SCA17	11.2
TSC22D4	11.1
PHAP I	11.1
ATXN7	11.1
SCA12	11.1
ANO10	11.0
SCA5	11.0
anoctamin 2	11.0
SPTBN2	10.9
SCA7	10.9
MAST4	10.8
PHF14	10.7
SCA1	10.6
SCA11	10.5
carbonic anhydrase-related protein	10.5
SCA3	10.5
SCA2	10.5
LAF4	10.5
KCNC3	10.5
SARA	10.5
excitatory amino acid transporter 4	10.4
WDR81	10.4
TOE1	10.3
PTPRR	10.3
protocadherin 10	10.2
B3GALNT2	10.2
ATXN10	10.1
Spinocerebellar ataxia type 7	10.1
ATXN3	10.0
CDG Ia	10.0

Disease
Cerebral ataxia	14.1
Cerebellum	14.1
Cerebellar Glioblastoma Multiforme	14.1
Progressive cerebellar ataxia	12.1
SCA23	12.1
SCA18	12.1
Rebound nystagmus	12.0
SCA25	11.8
SCA19	11.8
SCA14	11.8
SCAR8	11.8
Brainstem compression	11.8
SCA20	11.8
SCA21	11.5
SCA5	11.3
SCA13	11.2
SCA6	11.2
SCA17	11.2
SCA16	11.1
SCA12	11.1
SCA11	11.0
SCA7	10.8
SCA27	10.7
Spinocerebellar ataxia	10.6
SCA1	10.5
SCA2	10.5
Vertical nystagmus	10.3
SCA15	10.2
Neuhauser syndrome	10.2
Machado-Joseph disease	10.1
Fetal asphyxia	10.0
Age-associated memory impairment	10.0
Gaze-evoked nystagmus	9.9
SCA8	9.8
writing disorder	9.8
SCA4	9.7
Progressive myoclonic epilepsy	9.7
alcoholic cerebellar degeneration	9.3
cerebellar syndrome	9.3
AOA2	9.2

Symptom
poor balance and coordination	11.5
Limb ataxia	11.0
Apraxic	9.7
Ataxic	9.6
Pyramidal signs	9.5
cerebellar ataxia	9.4
Postural tremor	9.0
ataxia	8.9
abiotrophy	8.8
intention tremor	8.3
Cervical dystonia	7.5
ataxic gait	7.3
dysarthria	7.2
stump pain	7.2
astasia	7.2
loss of balance	6.9
frequent urination	6.7
clumsiness	6.6
Neurologic symptoms	6.6
impaired motor coordination	6.5
Extrapyramidal symptoms	6.5
giddiness	6.5
tremor	6.5
giddiness	6.5
incoordination	6.1
chorea	6.1
dystonia	6.1
Psychiatric symptoms	5.8
abnormal gait	5.6
myoclonus	5.4
muscle cramps	5.3
vertigo	5.1
ophthalmoplegia	5.0
urinary frequency	5.0
bradykinesia	4.9
partial seizure	4.7
spasticity	4.6
alexithymia	4.4
neurological disability	4.3
hypotonia	4.2

Enzyme
triokinase	9.0
m-AAA protease	8.6
ketohexokinase	8.4
UDP-galactose:ceramide galactosyltransferase	8.2
arylsulfate sulfotransferase	7.8
CDP-diacylglycerol synthase	7.5
SCP	7.3
VOR	6.8
alanyl-tRNA synthetase	6.4
sphingomyelin synthase	6.2
6-phosphofructo-2-kinase	5.8
inositol phosphatase	5.7
sulfite oxidase	5.3
sulfite oxidase	5.2
monoacylglycerol lipase	4.7
mu-calpain	4.7
sphingosine kinase	4.6
GABA transaminase	4.5
TSA	3.9
DAT	3.6
protein phosphatase 2A	3.6
paraoxonase	3.4
aldolase	3.4
aconitase	3.4
NOS	3.3
TdT	3.2
glutaminase	3.2
CaMKII	3.2
paraoxonase	3.1
histone acetyltransferase	2.7
5'-nucleotidase	2.5
sulfatase	2.5
caspase-8	2.4
tyrosine hydroxylase	2.3
PDE	2.3
caspase-9	2.3
PCP	2.3
glucose-6-phosphate dehydrogenase	2.2
NADPH-diaphorase	2.2
proteinase K	2.1