| Human Disease |
3-methylcrotonyl-Coa Carboxylase 1 Deficiency OMIM ID: 210200 |
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| Synonyms | 3-methylcrotonylglycinuria I; MCC1 Deficiency; Mccd Type 1; Methylcrotonylglycinuria Type I | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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