ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Hyperinsulinism due to INSR deficiency

Phakomatosis pigmentokeratotica


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	INSR	(0.67)	HRAS

Citations in the biomedical literature:

Hyperinsulinism due to INSR deficiency		Phakomatosis pigmentokeratotica
	Synonym(s): - Hyperinsulinemic hypoglycemia due to INSR deficiency - Hyperinsulinemic hypoglycemia due to insulin receptor deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare oncologic disease - Rare skin disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young 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: unknown

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 1 MeSH reference: C537893

No signs/symptoms info available.