UMLS:C0751651 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0751651 (mitochondrial disease)
1,844 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
MELAS	0.005
POLG	0.004
MERRF	0.003
EARS2	0.002
SURF1	0.001
EARS2 protein	0.001
sideroflexin 4	0.001
DNA polymerase gamma	0.001
LHON	0.001
C10orf2	0.001
MTND1	0.001
YARS2	0.001
complex I assembly factor	0.001
C20orf7	0.001
cytochrome c oxidase	0.001
MTND6	0.001
GFM1	0.001
CCDC44	0.001
TK2 protein	0.001
Succinate-CoA ligase, ADP-forming, beta subunit	0.001
C2orf64	0.001
NUCM	0.001
ATP6A	0.001
PRO1853	0.001
METT11D1	0.001
C1orf31	0.001
BOLA3 protein	0.001
FBXL4	0.001
COQ4	0.001
MTND3	0.001
MTATP6	0.001
NDUFAF1	0.001
MRPS22	0.001
SFRS8	0.001
ACAD9	0.001
ATP5SL	0.001
BCS1L	0.001
TTC19	0.001
RRM2B	0.000
SUCLA2	0.000

Disease
mitochondrial disease	0.999
Leigh syndrome	0.008
MELAS	0.007
Leber's hereditary optic neuropathy	0.007
MELAS	0.006
mitochondrial myopathy	0.006
lactic acidosis	0.006
mitochondrial encephalomyopathy	0.005
MERRF	0.003
Alpers	0.003
Kearns-Sayre syndrome	0.003
Chronic progressive external ophthalmoplegia	0.002
Complex I deficiency	0.002
Pearson's syndrome	0.001
myopathy	0.001
myoclonus epilepsy	0.001
encephalopathy	0.001
Complex III deficiency	0.001
Barth syndrome	0.000
mental developmental delay	0.000
Disorders of mitochondrial metabolism	0.000
Metabolic cardiomyopathy	0.000
SCAE	0.000
ATP synthase deficiency	0.000
CMTX4	0.000
Idiopathic growth hormone deficiency	0.000
cardiomyopathy	0.000
MILS	0.000
deafness	0.000
FRDA	0.000
optic atrophy	0.000
Friedreich's ataxia	0.000
MEHMO	0.000
Cytochrome c oxidase deficiency	0.000
sideroblastic anemia	0.000
Cone dystrophy	0.000
MNGIE	0.000
Mitochondrial DNA depletion	0.000
Mitochondrial neurogastrointestinal encephalopathy	0.000
developmental delay	0.000

Symptom
ophthalmoplegia	0.002
Sensory ataxia	0.000
Ophthalmoparesis	0.000
hypotonia	0.000
ataxia	0.000
External ophthalmoplegia	0.000
benign congenital hypotonia	0.000
seizures	0.000
weakness	0.000
Ataxic	0.000
cerebellar ataxia	0.000
dysarthria	0.000
myoclonus	0.000
Cold intolerance	0.000
muscle cramps	0.000
dystonia	0.000
Exercise intolerance	0.000
fatigue	0.000
impaired motor coordination	0.000
myalgia	0.000
spasticity	0.000
hyperemesis	0.000
hepatomegaly	0.000
lethargy	0.000
clumsiness	0.000
ataxic gait	0.000
ketonuria	0.000
hyperoxia	0.000
tonic-clonic seizure	0.000
paraparesis	0.000
partial seizure	0.000
headache	0.000
tremor	0.000
anesthesia	0.000
blurred vision	0.000
neurological disability	0.000
DNA marker	0.000
chorea	0.000
dysesthesia	0.000
sleepiness	0.000

Enzyme
complex I	0.002
cytochrome oxidase	0.000
succinate dehydrogenase	0.000
tRNA isopentenyltransferase	0.000
pyruvate dehydrogenase	0.000
sulfur dioxygenase	0.000
ATP synthase	0.000
acylglycerol kinase	0.000
GMP reductase	0.000
citrate synthase	0.000
glycerate kinase	0.000
pyruvate dehydrogenase	0.000
pyruvate dehydrogenase	0.000
NADH dehydrogenase	0.000
aspartyl-tRNA synthetase	0.000
rhomboid protease	0.000
DNA polymerase	0.000
tRNase Z	0.000
aconitase	0.000
deoxyguanosine kinase	0.000
RNase P	0.000
acyl-CoA dehydrogenase	0.000
thymidine phosphorylase	0.000
adenylosuccinate lyase	0.000
histidyl-tRNA synthetase	0.000
diaphorase	0.000
acyl-CoA dehydrogenase	0.000
phosphatidylserine decarboxylase	0.000
AMP-activated protein kinase	0.000
glutaryl-CoA dehydrogenase	0.000
alanyl-tRNA synthetase	0.000
PRPP synthetase	0.000
sulfhydryl oxidase	0.000
tryptophanyl-tRNA synthetase	0.000
phenylalanyl-tRNA synthetase	0.000
AMPK	0.000
biotinidase	0.000
succinyl-CoA synthetase	0.000
ornithine transcarbamylase	0.000
IscS	0.000