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
00003 RP (AD) Retinitis Pigmentosa (AD) - AD 12 0 BBS1, BEST1, CRX, DMPK, FSCN2, GUCA1A, IMPDH1, IMPG2, KIF21A, LCA5, MFN2, PRCD, PRPF3, PRPF6, RDH12, RHO, SEMA4A, TGFBI, USH2A, ZNF423 - -
00001 RP (AR) Retinitis Pigmentosa AR - AR 71 0 ABCA4, ABCC6, ADGRA3, ADGRV1, AHI1, AIPL1, ALMS1, ARL6, BBS1, BBS2, BBS4, BBS5, BBS7, BBS9, BEST1, CA4, CDH23, CDHR1, CEP164, CEP290, 76 more - -
00002 RP (XL) Retinitis Pigmentosa (X-linked) - XL 2 0 CHM, GPR143, MED12, OFD1, RP2, RPGR, RS1 - -
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