alpha-methylacyl-CoA racemase deficiency
Human disease
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Summary
alpha-methylacyl-CoA racemase deficiency is a rare disease[1].
Key Facts
- alpha-methylacyl-CoA racemase deficiency's instance of is recorded as rare disease[2].
- alpha-methylacyl-CoA racemase deficiency's instance of is recorded as class of disease[3].
- alpha-methylacyl-CoA racemase deficiency's subclass of is recorded as peroxisomal disease[4].
- alpha-methylacyl-CoA racemase deficiency's MeSH descriptor ID is recorded as C535444[5].
- alpha-methylacyl-CoA racemase deficiency's OMIM ID is recorded as 614307[6].
- alpha-methylacyl-CoA racemase deficiency's ICD-10 ID is recorded as K76.8[7].
- alpha-methylacyl-CoA racemase deficiency's KEGG ID is recorded as H02099[8].
- alpha-methylacyl-CoA racemase deficiency's Disease Ontology ID is recorded as DOID:0060602[9].
- alpha-methylacyl-CoA racemase deficiency's Orphanet ID is recorded as 79095[10].
- alpha-methylacyl-CoA racemase deficiency's health specialty is recorded as gastroenterology[11].
- alpha-methylacyl-CoA racemase deficiency's genetic association is recorded as AMACR[12].
- alpha-methylacyl-CoA racemase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060602[13].
- alpha-methylacyl-CoA racemase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0060602[14].
- alpha-methylacyl-CoA racemase deficiency's Medical Dictionary for Regulatory Activities ID is recorded as 10013234[15].
- alpha-methylacyl-CoA racemase deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- alpha-methylacyl-CoA racemase deficiency's Mondo ID is recorded as MONDO_0013681[17].
- alpha-methylacyl-CoA racemase deficiency's Genetics Home Reference Conditions ID is recorded as alpha-methylacyl-coa-racemase-deficiency[18].
- alpha-methylacyl-CoA racemase deficiency's UniProt disease ID is recorded as DI-00076[19].
- alpha-methylacyl-CoA racemase deficiency's Experimental Factor Ontology ID is recorded as 1001980[20].