ODCs

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

PROTEIN INTERACTIONS: 1

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

Hyperinsulinism due to INSR deficiency

Helicoid peripapillary chorioretinal degeneration


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	INSR	(0.63)	TEAD1

Citations in the biomedical literature:

Hyperinsulinism due to INSR deficiency		Helicoid peripapillary chorioretinal degeneration
	Synonym(s): - Hyperinsulinemic hypoglycemia due to INSR deficiency - Hyperinsulinemic hypoglycemia due to insulin receptor deficiency		Synonym(s): - Atrophia areata - SCRA - Sveinsson chorioretinal atrophy

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the eye and adnexa -

	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: <1 / 1 000 000 Average age onset: - 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.