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
02290 RP11 retinitis pigmentosa, type 11 (RP11) 600138 AD 0 0 PRPF31 - -
02361 RP18 retinitis pigmentosa, type 18 (RP18) 601414 - 0 0 PRPF3 - -
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