Disease #06622 (MTDPS12A (Mi DNA depletion syndrome 12A (cardiomyopathic type) AD), OMIM:617184)
| Official abbreviation |
MTDPS12A |
| Name |
Mi DNA depletion syndrome 12A (cardiomyopathic type) AD |
| OMIM ID |
617184 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC25A4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
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