ODCs

Click node...

1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
5 associated genes
No signs/symptoms info

Autosomal dominant hyperinsulinism due to SUR1 deficiency

Permanent neonatal diabetes mellitus

Citations in the biomedical literature:

Autosomal dominant hyperinsulinism due to SUR1 deficiency		Permanent neonatal diabetes mellitus
	Synonym(s): - Autosomal dominant hyperinsulinemic hypoglycemia due to SUR1 deficiency		Synonym(s): - PNDM

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Certain conditions originating in the perinatal period -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.