Disease #04343 (CBAS-5 (bile acid synthesis defect?, congenital, type 5 (CBAS-5)), OMIM:616278)

Official abbreviation CBAS-5
Name bile acid synthesis defect?, congenital, type 5 (CBAS-5)
OMIM ID 616278
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ABCD3
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited N/A