All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03456 LCA8 Leber congenital amaurosis, type 8 (LCA-8) 613835 - 0 0 CRB1 - -
01507 PPCRA atrophy, chorioretinal, pigmented paravenous (PPCRA) 172870 AD 5 5 CRB1 - -
02286 RP12 retinitis pigmentosa, with/without PPRPE, type 12 (RP12) 600105 AR 12 12 CRB1 - -
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