Disease #06585 (MC1DN31 (Mi complex I deficiency, nuclear type 31), OMIM:618251)
Official abbreviation |
MC1DN31 |
Name |
Mi complex I deficiency, nuclear type 31 |
OMIM ID |
618251 |
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 |
TIMMDC1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|