All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03444 CBAS3 bile acid synthesis defect, congenital, type 3 (CBAS-3) 613812 AR - - CYP7B1 - -
02078 SPG5A paraplegia, spastic, autosomal recessive, type 5A (SPG-5A) 270800 AR 5 5 CYP7B1 - -
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