Disease #04455 (ECHS1D (enoyl-CoA hydratase 1 deficiency, short-chain, mitochondrial (ECHS1D)), OMIM:616277)
| Official abbreviation |
ECHS1D |
| Name |
enoyl-CoA hydratase 1 deficiency, short-chain, mitochondrial (ECHS1D) |
| OMIM ID |
616277 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
6 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
ECHS1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2020-07-09 13:43:10 +02:00 (CEST) |
Individuals
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