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
01471 CSNBAD-2 blindness, night, stationary, congenital, autosomal dominant, type 2 (CSNBAD-2) 163500 - 0 0 PDE6B - -
03440 RP-40 retinitis pigmentosa, type 40 (RP-40) 613801 - 0 0 PDE6B - -
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