All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05926 ARB Bestrophinopathy, autosomal recessive (ARB) 611809 AR 2 2 BEST1 - -
00112 RP retinitis pigmentosa (RP) 268000 - 1159 897 ADCK4, ARL3, BEST1, CC2D2A, CNGB1, DHDDS, EYS, HKDC1, IDH3A, IMPG1, KIF3B, NR2E3, POC5, PRPF8, RNU4-2, RNU6-1, RNU6-2, RNU6-8, RNU6-9, SLC7A14, SMG8, TMEM216 - -
03279 RP50 retinitis pigmentosa, type 50, concentric (RP50) 613194 - 1 - BEST1 - -
01424 VMD dystrophy, macular, vitelliform (VMD) - - 8 7 BEST1, IMPG1, IMPG2, PRPH2 - -
03059 VMD2 dystrophy, macular, vitelliform, type 2 (VMD-2 (Best macular dystrophy (BMD)) 153700 AD 2 2 BEST1 - -
01600 VRCP;MRCS2 vitreoretinochoroidopathy (VRCP, MRCS2 included) 193220 AD - - BEST1 - -
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