All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04212 BBS Bardet-Biedl syndrome (BBS) - - 282 240 ARL6, BBS9, C8orf37, IFT74 - -
04364 BBS3 Bardet-Biedl syndrome, type 3 (BBS-3) 600151 AR 1 1 ARL6 - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
00888 RP55 retinitis pigmentosa, type 55 (RP55) 613575 - - - ARL6 - -
04048 SPG61 paraplegia, spastic, type 61, autosomal recessive (SPG-61) 615685 AR 3 3 ARL6IP1 - -
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