Disease #00009 (MCADD (Medium-chain Acyl-CoA dehydrogenase deficiency), OMIM:607008)
| Official abbreviation |
MCADD |
| Name |
Medium-chain Acyl-CoA dehydrogenase deficiency |
| OMIM ID |
607008 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ACADM |
| Associated tissues |
liver |
| Disease features |
- |
| Remarks |
- |
|
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