Disease #03243 (MPMCD (myopathy, mitochondrial progressive, with congenital cataract and developmental delay), OMIM:613076)
| Official abbreviation |
MPMCD |
| Name |
myopathy, mitochondrial progressive, with congenital cataract and developmental delay |
| OMIM ID |
613076 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
GFER |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-01-14 16:06:18 +01:00 (CET) |
Individuals
|