ODCs

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

PROTEIN INTERACTIONS: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Hyperinsulinism due to INSR deficiency

Generalized arterial calcification of infancy

INSR	(UniProt - OMIM)		ABCC6	(UniProt - OMIM)
			ENPP1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	INSR	(0.89)	ENPP1

Citations in the biomedical literature:

Hyperinsulinism due to INSR deficiency		Generalized arterial calcification of infancy
	Synonym(s): - Hyperinsulinemic hypoglycemia due to INSR deficiency - Hyperinsulinemic hypoglycemia due to insulin receptor deficiency		Synonym(s): - Idiopathic infantile arterial calcification - Idiopathic obliterative arteriopathy - Infantile arteriosclerosis - Occlusive infantile arteriopathy

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease		Classification (Orphanet): - Rare circulatory system disease - Rare genetic 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: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C537440

No signs/symptoms info available.