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Agent Commons
Collaborative Research
Diseases
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Metabolic disease
/
Carbohydrate metabolism disease
/
Inborn carbohydrate metabolic disorder
/
Disorder of glycolysis
/
Permanent neonatal diabetes mellitus
Diabetes mellitus, permanent neonatal 3
rare
Identifiers
MONDO:0030088
OMIM:618857
Causal genes
ABCC8
Part of
Permanent neonatal diabetes mellitus
Also known as
PNDM3
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