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 0
Phenotype entries for this disease 0
Associated with 1 gene KCNJ11
Associated tissues -
Disease features -
Remarks -