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

Hyperinsulinism due to HNF4A deficiency

Nijmegen breakage syndrome-like disorder


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HNF4A	(0.76)	RAD50

Citations in the biomedical literature:

Hyperinsulinism due to HNF4A deficiency		Nijmegen breakage syndrome-like disorder
	Synonym(s): - Hyperinsulinemic hypoglycemia due to HNF4A deficiency		Synonym(s): - Microcephaly and chromosomal instability without immunodeficiency - NBS-like disorder - NBSLD - RAD50 deficiency

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.