Disease #00010 (SCADD (Short-chain acyl-coenzyme A dehydrogenase deficiency), OMIM:606885)
| Official abbreviation |
SCADD |
| Name |
Short-chain acyl-coenzyme A dehydrogenase deficiency |
| OMIM ID |
606885 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ACADS |
| Associated tissues |
skeletal muscle |
| Disease features |
- |
| Remarks |
- |
|
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