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

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00465968 334974 - - M likely Saudi Arabia - - - - - PNDM1 Diabetes mellitus, Elevated hemoglobin A1c, Reduced C-peptide level GCK GCK 1 1 Andreas Laner
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