UMLS:C0029089 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0029089 (ophthalmoplegia)
3,338 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

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Human Gene/Protein
CFEOM2	12.9
ZNF541	12.2
SUCLA1	12.2
IOSCA	12.2
CFEOM1	12.0
C10orf2	11.9
SANDO	11.9
Mitochondrial DNA polymerase gamma	11.8
C20orf72	11.6
MNGIE	11.2
KIF21A	11.1
MYH2	11.0
polg	10.9
TWINKLE	10.9
POLG	10.7
MEIS3	10.6
RNASEH1	10.6
RRM2B	10.5
PolB	10.5
acetylcholine receptor epsilon subunit	10.4
DNA polymerase gamma	10.4
SLC8A2	10.2
kinesin family member 21A	10.2
Dihydropyridine receptor	10.2
PHOX2A	10.1
LRP12	9.9
mtRF1a	9.9
DGUOK	9.9
ECGF1	9.8
DHX34	9.8
Spinocerebellar ataxia 7	9.8
AAC2	9.7
SCA11	9.6
POLG protein	9.6
MERRF	9.5
AAC1	9.5
TSFM	9.5
MPV17	9.5
SLC10A3	9.4
SUCLA2	9.4

Disease
Nothnagel's syndrome	13.2
Deficiency of thymidine phosphorylase	13.2
Abducting nystagmus	13.2
Jacod's syndrome	13.2
IBM3	13.2
necrotic intraocular melanoma	13.2
Idiopathic dermatomyositis	13.2
CFEOM2	13.2
One-and-a-half syndrome	13.2
Supranuclear ophthalmoplegia	12.6
Orbital apex syndrome	12.4
Internuclear ophthalmoplegia	12.3
Neuroparalytic keratitis	12.2
Supranuclear gaze palsy	12.2
DURS2	12.2
CFEOM1	12.2
Intranuclear Ophthalmoplegia	12.2
Dissociated nystagmus	12.2
Familial visceral neuropathy	12.2
Mitochondrial neurogastrointestinal encephalopathy	12.2
Painful ophthalmoplegia	12.1
Tolosa-Hunt syndrome	12.1
Ophthalmoplegic migraine	12.1
Cavernous sinus syndrome	12.1
IOSCA	12.0
SANDO	11.9
Miller Fisher syndrome	11.8
CFEOM3	11.8
Nummular keratitis	11.6
Other myopathies	11.6
Other myopathies	11.6
Kearns-Sayre syndrome	11.5
Chronic progressive external ophthalmoplegia	11.4
Progressive cerebellar ataxia	11.2
SCA18	11.2
Total ophthalmoplegia	11.2
Bulbar weakness	11.2
SCA26	11.2
MNGIE	11.2
Sphenoidal sinus	11.1

Symptom
Doll's eye sign	13.2
ophthalmoplegia	13.2
Internal ophthalmoplegia	12.6
Ophthalmalgia	12.2
Ophthalmoparesis	11.4
External ophthalmoplegia	11.4
Periorbital pain	11.2
Limb weakness	11.1
Retro-orbital pain	10.9
Sensory ataxia	10.7
Bell's phenomenon	10.6
Limb ataxia	10.1
Muscle fibrosis	9.9
Sudden loss of vision	9.9
sense loss	9.9
Truncal ataxia	9.9
Ataxic	9.7
Nuchal rigidity	9.2
benign congenital hypotonia	9.1
hemihypesthesia	8.6
eye pain	8.5
ataxic gait	8.4
ataxia	8.4
Thunderclap headache	8.3
cerebellar ataxia	8.2
Convergence Insufficiency	8.2
Intractable pain	8.1
polyopia	8.1
athetosis	8.0
dysarthria	8.0
asterixis	7.8
Kernig's sign	7.6
periorbital edema	7.6
paresis	7.5
Exercise intolerance	7.4
Fatigability	7.2
clumsiness	7.1
consciousness disturbance	7.1
staggering gait	7.1
skin pain	7.0

Enzyme
deoxyguanosine kinase	8.9
thymidine phosphorylase	8.1
RPH	7.5
GMP reductase	7.4
peptidyl-tRNA hydrolase	6.5
CYP7B1	6.3
VOR	5.9
pantothenate kinase	5.3
complex I	5.0
cytochrome oxidase	4.8
sialyltransferase	4.6
sialyltransferase	4.6
sialyltransferase	4.6
succinate dehydrogenase	4.6
biotinidase	4.6
dihydropteridine reductase	4.6
succinyl-CoA synthetase	4.5
DNA polymerase	4.5
carnitine acetyltransferase	4.5
NADH dehydrogenase	4.5
transketolase	4.5
glucosylceramide synthase	4.3
pyruvate dehydrogenase	4.3
pyruvate dehydrogenase	4.0
pyruvate dehydrogenase	4.0
diaphorase	4.0
arylsulfatase A	3.9
endothelin-converting enzyme	3.9
TPP	3.9
GCA	3.8
TPP	3.7
Alternating	3.6
TMT	3.6
pyruvate decarboxylase	3.5
succinic dehydrogenase	3.5
phosphorylase kinase	3.4
LasR	3.4
ribonucleotide reductase	3.3
creatine kinase	3.3
ribonucleotide reductase	3.3