ODCs

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

COMMON GENES: 1

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

Autosomal dominant hyperinsulinism due to Kir6.2 deficiency

Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency

Citations in the biomedical literature:

Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
	Synonym(s): - Autosomal dominant hyperinsulinemic hypoglycemia due to Kir6.2 deficiency		Synonym(s): - Hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, diazoxide-resistant focal form

	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): - Endocrine, nutritional and metabolic diseases -

	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: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.