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Disease Ontology Browser
amino acid metabolic disorder (DOID:9252)
Alliance: disease page
Synonyms: inborn errors of amino acid metabolism
Alt IDs: ICD10CM:E72.9, ICD9CM:270, ICD9CM:270.9, MESH:D000592, NCI:C97090, UMLS_CUI:C0002514
Definition: An inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids.

Disease References using Mouse Models (122)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory