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DO Term : permanent neonatal diabetes mellitus [DOID:0060639] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A neonatal diabetes that has_material_basis_in homozygous mutation in the glucokinase gene (GCK), heterozygous mutation in the KCNJ11 and INS genes, or by heterozygous or homozygous mutation in the ABCC8 gene.
  • synonyms:
  • PDMI,
  • GARD:10457,
  • PNDM,
  • permanent diabetes mellitus of infancy,
  • OMIM:606176,
  • 606176
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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