ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Phakomatosis pigmentokeratotica

Hyperinsulinism due to INSR deficiency


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

Citations in the biomedical literature:

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

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		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: unknown		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.