|
DOID:9252 - amino acid metabolic disorder
Disease Ontology Definition:An inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids.
Synonyms: inborn errors of amino acid metabolism
Xenbase Genes
:
prdx1,
slc22a5,
slc25a1,
amt,
opa3,
aass,
pepd,
fh,
pcca,
gamt,
ggt1,
ahcy,
psph,
bckdhb,
hpd,
| MONDO:0004736 - metanephric glomerulus |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
inherited metabolic disorder (is_a)