Disease #00529
Official abbreviation |
616277 |
Name |
Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency, 616277 (3) |
OMIM ID |
616277 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
ECHS1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|