ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome

Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RFX6	(0.63)	ARNT2

Citations in the biomedical literature:

Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome		Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies

	Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.