# permanent neonatal diabetes mellitus

> neonatal diabetes mellitus 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

**Wikidata**: [Q17143640](https://www.wikidata.org/wiki/Q17143640)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Permanent_neonatal_diabetes)  
**Source**: https://4ort.xyz/entity/permanent-neonatal-diabetes-mellitus


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/9c21ba4d-785f-486f-84f8-511b9c89c137--2020-05-13T16:00:00)
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_9c21ba4d-785f-486f-84f8-511b9c89c137-2020-05-13T160000.000Z)
6. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)
7. UMLS 2023