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
05352 BCS cornea, brittle, syndrome (BCS) - - 16 16 PRDM5, ZNF469 - -
01792 BCS1 cornea, brittle, syndrome, type 1 (BCS-1, corneal fragility keratoglobus, blue sclerae and joint hypermobility) 229200 AR 1 1 ZNF469 - -
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