Disease #03011 (MC1DN20 (mitochondrial complex I deficiency, nuclear type 20 (MC1DN20, acyl-CoA dehydrogenase family 9 deficiency)), OMIM:611126)
| Official abbreviation |
MC1DN20 |
| Name |
mitochondrial complex I deficiency, nuclear type 20 (MC1DN20, acyl-CoA dehydrogenase family 9 deficiency) |
| OMIM ID |
611126 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ACAD9 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-05-19 07:44:35 +02:00 (CEST) |
Individuals
|