Disease #00159 (MDPL (MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME), OMIM:615381)
| Official abbreviation |
MDPL |
| Name |
MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME |
| OMIM ID |
615381 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
POLD1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2023-06-27 11:12:18 +00:00 (UTC) |
| Date last edited |
N/A |
|
|
