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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