UMLS:C0235394 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0235394 (wasting)
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Human Gene/Protein
PHA1	11.0
transient receptor potential cation channel, subfamily M, member 6	11.0
ALKALI	11.0
dystrophin, muscle	10.6
TUBB4Q	10.4
CCL25 protein	10.4
Na+/H+ exchanger isoform 2	10.0
CYP21A2 protein	10.0
FLJ10737	10.0
SLC17A2	10.0
CAPN3 protein	10.0
D6Mm5e	10.0
HSAN II	9.8
PHEX	9.7
bicaudal D homolog 2	9.6
PiUS	9.6
CYP21 protein	9.6
DNAJC11	9.6
NPT2	9.6
calcium binding protein 39	9.6

Disease
Carnitine uptake deficiency	12.0
Osteogenesis imperfecta type IV	12.0
SPPK1	12.0
Infection by Trypanosoma vivax	12.0
Hypercalciuric rickets	12.0
Branchitis	12.0
Nutritional stunting	12.0
wasting	12.0
Renal magnesium wasting	11.5
Primary hypomagnesemia	11.1
CMO II deficiency	11.1
Diabetic amyotrophy	11.0
CMT4H	11.0
FAB type M5a	11.0
West Nile encephalomyelitis	11.0
HMN V	11.0
Chronic hepatic failure	11.0
Lignac	11.0
Man-in-the-barrel syndrome	11.0
Hypokalemic hypochloremic metabolic alkalosis	11.0

Enzyme
corticosterone methyl oxidase	9.6
KDOP synthase	9.4
21-hydroxylase	8.5
calpain 3	7.3
calpain 3	7.0
methylmalonate-semialdehyde dehydrogenase	7.0
3-hydroxyisobutyrate dehydrogenase	6.7
cholesterol 25-hydroxylase	6.5
UDP-N-acetylglucosamine 2-epimerase	6.2
3beta-hydroxysteroid dehydrogenase	5.7
amylo-1,6-glucosidase	5.6
galactosylhydroxylysyl glucosyltransferase	5.6
matrix metalloproteinase 14	5.5
STK2	5.4
nicotinamide N-methyltransferase	5.4
adenylosuccinate lyase	5.4
phosphoglycolate phosphatase	5.4
branched-chain alpha-keto acid dehydrogenase	5.3
adenine deaminase	5.3
phosphatidylglycerophosphate synthase	5.3