3-methylcrotonyl-CoA carboxylase 2 deficiency Disease Ontology Browser

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Disease Ontology Browser

3-methylcrotonyl-CoA carboxylase 2 deficiency (DOID:0080580)
Alliance: disease page
Alt IDs: OMIM:210210, MESH:C535309
Definition: A 3-Methylcrotonyl-CoA carboxylase deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the beta subunit of 3-methylcrotonyl-CoA carboxylase on chromosome 5q13.

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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