UMLS:C0848771 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0848771 (neurological disability)
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Human Gene/Protein
SH3BP4	11.7
KLHL13	11.7
2',3'-cyclic nucleotide 3' phosphodiesterase	11.6
protein tyrosine phosphatase receptor type C	11.6
HSPA4L	11.5
NEXN	11.4
HARS2	11.1
RRN3	10.8
N-acetylglucosamine-6-O-sulfotransferase	10.8
tetraspan membrane protein	10.7
EPB41L4A	10.7
LARS2	10.5
Po protein	10.4
DNAJC12	10.4
POLR1D	10.4
sphingomyelin synthase 1	10.4
14-3-3 epsilon protein	10.1
ST3GAL5	10.1
SOS-1	10.1
RPL3	10.0

Disease
Multidirectional nystagmus	15.1
Tumorlet	13.1
Progressive multiple sclerosis	12.5
Secondary progressive multiple sclerosis	11.6
Adhesive arachnoiditis	11.6
Spinal cord atrophy	11.5
Retinal atrophy	11.3
Demyelinating disorders	10.7
Hypoxic-ischemic brain injury	10.7
Progressive myoclonic epilepsy	10.7
Primary progressive multiple sclerosis	10.3
triplegia	10.2
Acute posterior multifocal placoid pigment epitheliopathy	10.2
Intermediate uveitis	10.1
Cryptococcal infections	10.1
Reversible posterior leukoencephalopathy syndrome	10.0
Neonatal meningitis	10.0
Cavernous sinus thrombosis	9.9
Balo's concentric sclerosis	9.8
Cervical myelopathy	9.7

Enzyme
GalNAc-T	8.3
GM3 synthase	7.3
NCP	7.1
esterase D	7.1
S-adenosyl-L-homocysteine hydrolase	7.0
DMT	6.1
isopeptidase	5.9
phenylalanine hydroxylase	5.6
gamma-glutamylcysteine synthetase	5.6
GAS	5.2
nucleotidase	5.1
tissue plasminogen activator	4.8
acyl-CoA synthetase	4.7
indoleamine 2,3-dioxygenase	4.6
3-hydroxy-3-methylglutaryl coenzyme A reductase	4.6
aconitase	4.3
botulinum neurotoxin	4.2
PDK1	3.9
matrix metalloproteinase 2	3.9
TAT	3.8