Disease #00092 (PNDM1 (DIABETES MELLITUS, PERMANENT NEONATAL, 1), OMIM:606176)

Official abbreviation PNDM1
Name DIABETES MELLITUS, PERMANENT NEONATAL, 1
OMIM ID 606176
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GCK
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 09:18:18 +00:00 (UTC)
Date last edited N/A

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