Disease #00040 (MTDPS7 (mitochondrial DNA depletion syndrome (hepatocerebral), type 7 (MTDPS-7)), OMIM:271245)
| Official abbreviation |
MTDPS7 |
| Name |
mitochondrial DNA depletion syndrome (hepatocerebral), type 7 (MTDPS-7) |
| OMIM ID |
271245 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
C10orf2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-08-30 16:45:18 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|