Disease #00061 (PNDM3 (DIABETES MELLITUS, PERMANENT NEONATAL, 3), OMIM:618857)
| Official abbreviation |
PNDM3 |
| Name |
DIABETES MELLITUS, PERMANENT NEONATAL, 3 |
| OMIM ID |
618857 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ABCC8 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2023-06-16 08:14:56 +00:00 (UTC) |
| Date last edited |
2023-06-16 08:26:55 +00:00 (UTC) |
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