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
02225 BCM monochromacy, blue cone (BCM, cone dystrophy, type 5 (COD-5)) 303700 XLR - - OPN1LW, OPN1MW - X-linked recessive
02227 CBP colorblindness, partial, Protan series (CBP) 303900 XL - - OPN1LW - X-linked
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