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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