UMLS:C0016719 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0016719 (Friedreich's ataxia)
2,098 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
mature T-cell proliferation 1	13.9
STM7	13.6
Frataxin	13.6
frataxin	13.6
FRDA	13.3
GAA1	12.6
ISD11	12.4
NFS1	11.9
GAA	11.9
H2AFY2	11.9
IOSCA	11.9
MTIF2	11.9
ATLD	11.6
PMPCA	11.6
ISCU	11.4
DCYTB	11.3
SCA7	11.0
PIP5K1B	11.0
lipoic acid-containing protein	10.9
FARS	10.8
mitochondrial ferritin	10.8
GRX5	10.7
SACS	10.7
pitrilysin metallopeptidase 1	10.6
SANDO	10.6
SCA2	10.5
SCA12	10.5
RNF126	10.5
MRS3/4	10.5
FAD1	10.4
CMTX5	10.4
GLRX5	10.4
SCA10	10.3
PRKACG	10.3
CT51	10.3
TGM6	10.3
cysteine desulfurase	10.3
putative DNA binding protein	10.3
Caytaxin	10.3
POLG protein	10.3

Disease
Friedreich's ataxia	13.9
Gaze palsy	13.9
FRDA2	13.9
Temporal pallor	13.9
FRDA	13.5
Early Onset Cerebellar Ataxia	13.3
Early onset cerebellar ataxia with retained tendon reflexes	13.2
Sanger-Brown	12.9
CMT2A2	12.9
Marie's ataxia	12.3
hereditary ataxia	12.2
IOSCA	12.1
SCAE	11.9
ATLD	11.9
Roussy-Levy	11.9
SCA25	11.6
FRA12A	11.6
Spastic ataxia	11.6
Ocular siderosis	11.3
HMSN VI	11.2
FARR	11.1
AOA2	11.0
SCA7	11.0
SCA23	10.9
SCA16	10.9
Spinocerebellar degeneration	10.7
alcoholic cerebellar degeneration	10.7
CMTX5	10.6
SANDO	10.6
SCA12	10.5
SCA6	10.5
SCA2	10.5
Duchenne's disease	10.4
SCA5	10.3
X-linked sideroblastic anemia	10.3
VED	10.2
olivopontocerebellar atrophy	10.1
SCA1	10.1
SCA15	10.0
Neuromuscular scoliosis	10.0

Symptom
poor balance and coordination	12.3
urgent urination	12.3
Ataxic	9.3
Pyramidal signs	9.3
cerebellar ataxia	9.1
ataxia	9.0
dysarthria	8.2
ataxic gait	8.1
inanition	7.1
neurological disability	6.6
exertional chest pain	6.6
abnormal gait	6.6
intention tremor	6.4
impaired motor coordination	6.3
chorea	6.2
paraparesis	5.9
athetosis	5.9
male subfertility	5.8
ophthalmoplegia	5.8
spasticity	5.7
DNA marker	5.6
incoordination	5.4
dystonia	5.4
loss of balance	5.1
clumsiness	4.8
Gastrointestinal symptoms	4.7
myoclonus	4.6
pallor	4.6
tremor	4.5
CSR	4.5
clonus	4.4
hypotonia	4.2
weakness	4.1
bradykinesia	3.7
thinning	3.6
hypertonia	3.6
hyperoxia	3.5
asthenia	2.5
memory loss	2.1
apathy	1.9

Enzyme
valine dehydrogenase	11.0
IscS	9.8
aconitase	9.2
pantothenate kinase	9.1
phosphoethanolamine cytidylyltransferase	8.9
NADH kinase	8.6
electron transfer flavoprotein dehydrogenase	8.1
ethanolamine kinase	7.9
dihydrolipoamide succinyltransferase	7.7
3-hydroxy-3-methylglutaryl-CoA lyase	7.6
ferrochelatase	7.4
coproporphyrinogen oxidase	6.9
biliverdin reductase	6.8
LipA	6.7
diaphorase	6.5
Lod	6.3
PIP kinase	6.2
SCP	6.1
PDH	6.1
MPP	6.0
pyruvate dehydrogenase	5.7
succinate dehydrogenase	5.7
pyruvate dehydrogenase	5.4
pyruvate dehydrogenase	5.4
alpha-L-iduronidase	5.3
fumarase	5.3
biotinidase	5.3
pyruvate decarboxylase	5.2
alpha-ketoglutarate dehydrogenase	5.2
complex I	5.0
TRS	4.9
citrate synthase	4.8
isopeptidase	4.7
lecithin:cholesterol acyltransferase	4.7
porphobilinogen deaminase	4.6
polynucleotide kinase	4.5
acyl-CoA dehydrogenase	4.4
ceruloplasmin	4.4
TOR	4.4
rhodanese	4.4