Disease #00061 (PNDM3 (DIABETES MELLITUS, PERMANENT NEONATAL, 3), OMIM:618857)

Official abbreviation PNDM3
Name DIABETES MELLITUS, PERMANENT NEONATAL, 3
OMIM ID 618857
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ABCC8
Associated tissues -
Disease features -
Remarks -

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