Disease #06156 (PNDM2 (Diabetes, permanent neonatal 2, with or without neurologic features), OMIM:618856)
| Official abbreviation |
PNDM2 |
| Name |
Diabetes, permanent neonatal 2, with or without neurologic features |
| OMIM ID |
618856 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
KCNJ11 |
| 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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