Disease #00322 (MTDPS5 (mitochondrial DNA depletion syndrome, type 5 (MTDPS-5, encephalomyopathic with/without methylmalonic aciduria)), OMIM:612073)
| Official abbreviation |
MTDPS5 |
| Name |
mitochondrial DNA depletion syndrome, type 5 (MTDPS-5, encephalomyopathic with/without methylmalonic aciduria) |
| OMIM ID |
612073 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
SUCLA2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-02-02 22:41:39 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|