All diseases

11 entries on 1 page. Showing entries 1 - 11.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02029 - progesterone resistance 264080 - 0 0 PGR - -
02156 - retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness 300455 - 0 0 RPGR - -
02188 - degeneration, macular, X-linked atrophic 300834 - 0 0 RPGR - -
00076 COACH COACH syndrome 216360 - 1 1 CC2D2A, RPGRIP1L, TMEM67 - -
02743 CORD-13 dystrophy, cone-rod, type 13 (CORD-13) 608194 - 0 0 RPGRIP1 - -
02228 CORDX-1 dystrophy, cone-rod, X-linked, type 1 (CORDX-1) 304020 - 0 0 RPGR - -
00080 JBTS-7 Joubert syndrome, type 7 (JBTS-7) 611560 - 0 0 RPGRIP1L - -
03450 LCA-6 Leber congenital amaurosis, type 6 (LCA-6) 613826 - 0 0 RPGRIP1 - -
00079 MKS-5 Meckel syndrome, type 5 (MKS-5) 611561 - 0 0 RPGRIP1L - -
02138 RP-3 retinitis pigmentosa, type 3 (RP-3) 300029 - 0 0 RPGR - -
05426 XLRP retinitis pigmentosa, X-linked (XLRP) - - 23 23 RP2, RPGR - -
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