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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