ODCs

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

COMMON GENES: 1

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

Low phospholipid associated cholelithiasis

Progressive familial intrahepatic cholestasis type 3

Citations in the biomedical literature:

Low phospholipid associated cholelithiasis		Progressive familial intrahepatic cholestasis type 3
	Synonym(s): - ABCB4 gene mutation-associated cholelithiasis - Cholelithiasis with ABCB4 gene mutation		Synonym(s): - PFIC3

	Classification (Orphanet): - Rare genetic disease - Rare hepatic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hepatic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the digestive system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535935

No signs/symptoms info available.