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 HNF1A deficiency

Rubinstein-Taybi syndrome due to 16p13.3 microdeletion


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HNF1A	(0.88)	CREBBP

Citations in the biomedical literature:

Hyperinsulinism due to HNF1A deficiency		Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
	Synonym(s): - Hyperinsulinemic hypoglycemia due to HNF1A deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare renal 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: 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.