Disease #05783 (PNDM1 (diabetes mellitus, permanent neonatal, type 1 (PNDM1)), OMIM:606176)
Official abbreviation |
PNDM1 |
Name |
diabetes mellitus, permanent neonatal, type 1 (PNDM1) |
OMIM ID |
606176 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
GCK |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2020-07-09 17:00:59 +02:00 (CEST) |
Date last edited |
N/A |
Individuals
|