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Permanent neonatal diabetes mellitus 1
rareA rare autosomal recessive disorder characterized by severe hyperglycemia which requires insulin treatment soon after birth. The disorder results from a complete lack of glucokinase; total absence of basal insulin release was observed as well.
- Identifiers
- MONDO:0100165 OMIM:606176
- Causal genes
- GCK
- Also known as
- diabetes mellitus, permanent neonatal 1 · PDMI · PNDM1
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