UMLS:C0162671 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0162671 (MELAS)
587 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	455
tRNA	133
MERRF	108
Mol	47
Sep	45
MRI	43
cytochrome c oxidase	32
LHON	30
NARP	28
ATP	26
insulin	18
She	17
CADASIL	13
TL1A	12
ND5	11
cytochrome	11
NADH	10
pyruvate dehydrogenase complex	10
POLG	9
MNGIE	9
CSF	9
pyruvate dehydrogenase	8
axonal	8
ND1	7
X-linked	6
SDH	6
PEO	6
ND6	6
frataxin	6
NIDDM	5
OXPHOS	5
osteosarcoma	5
COX	5
ND4	5
Polymerase	4
nitric oxide synthase	4
ADP	4
NAD	4
IOSCA	4
polypeptide	4
creatine kinase	4
MRS	4
DNA polymerase gamma	4
SANDO	4
N-acetylaspartate	4
DARS2	4
Humanin	3
ATP synthase	3
Pol	3
cytochrome c	3
citrate synthase	3
COL4A1	3
caspase-3	3
WFS1	3
endonuclease	3
NADH-ubiquinone reductase	3
AHS	3
complex I)	3
glucagon	3
ubiquinone	3
POLG protein	3
ATPase 6	2
cardiac muscle	2
STAT3	2
oxidoreductase	2
EPI	2
cytochrome aa3	2
ROS	2
ATPase	2
AED	2
platelet-derived	2
Barth syndrome	2
ENT	2
NMR	2
PDC	2
Pyruvate dehydrogenase	2
IGFBP3	2
ALD	2
Q10	2
MnSOD	2

Disease
MELAS	587
MELAS	458
stroke	311
lactic acidosis	297
encephalopathy	203
mitochondrial myopathy	144
mitochondrial encephalomyopathy	112
MERRF	108
diabetes	89
mitochondrial disease	88
Leigh syndrome	62
epilepsy	58
myopathy	56
deafness	51
Kearns-Sayre syndrome	50
Leber's hereditary optic neuropathy	43
migraine	30
dementia	29
cardiomyopathy	27
Chronic progressive external ophthalmoplegia	25
hemiparesis	20
neuropathy	18
sensorineural hearing loss	17
myoclonus epilepsy	17
vascular disease	14
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy	14
fits	14
status epilepticus	14
CADASIL	13
aphasia	11
type 2 diabetes	11
Alzheimer's disease	10
retinitis pigmentosa	10
cognitive impairment	10
MNGIE	9
Parkinson's disease	9
Alpers	9
hypertrophic cardiomyopathy	8
leukoencephalopathy	8
Friedreich's ataxia	8
cerebral infarction	8
brain atrophy	8
developmental delay	8
prolapse	8
neurological disease	7
retinopathy	7
optic atrophy	7
encephalitis	6
blindness	6
mental retardation	6
hypertension	6
ischemia	6
glomerulosclerosis	5
glucose intolerance	5
osteosarcoma	5
psychosis	5
mental retardation	5
cancer	5
depression	5
MRS	4
arteriopathy	4
muscular atrophy	4
Wolfram syndrome	4
apraxia	4
tumor	4
renal disease	4
coma	4
malignant hyperthermia	4
hemiplegic migraine	4
peripheral neuropathy	4
IOSCA	4
SANDO	4
dilated cardiomyopathy	3
enzyme deficiency	3
CARASIL	3
heart failure	3
multiple sclerosis	3
acute renal failure	3
diabetic ketoacidosis	3
congestive heart failure	3

Enzyme
complex I	52
cytochrome oxidase	16
pyruvate dehydrogenase	16
succinate dehydrogenase	14
pyruvate dehydrogenase	8
pyruvate dehydrogenase	8
superoxide dismutase	4
citrate synthase	4
diaphorase	4
creatine kinase	4
LasR	3
CPT	3
alpha-ketoglutarate dehydrogenase	3
ATP synthase	3
endonuclease	3
ATPase	3
succinic dehydrogenase	2
acetylcholinesterase	2
fumarase	2
cholinesterase	2
mitogen-activated protein kinase	2
CPR	2
catalase	2
thymidine phosphorylase	2
NADH dehydrogenase	2
DNA polymerase	2
leucyl-tRNA synthetase	2
thyroid peroxidase	1
branched-chain alpha-keto acid dehydrogenase	1
phosphoinositide 3-kinase	1
diaphorase	1
glutathione peroxidase	1
RNase	1
glutamate decarboxylase	1
thrombin	1
CPT	1
ceruloplasmin	1
acyl-CoA dehydrogenase	1
caspase-3	1
NO synthase	1
pyruvate carboxylase	1
AMP-activated protein kinase	1
argininosuccinate synthetase	1
acetyl-CoA carboxylase	1
phosphorylase	1
aconitase	1
NADPH-diaphorase	1
RNase	1
phosphoglycerate kinase	1
HVS	1
biotinidase	1
CPT	1
calcineurin	1