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
00089 BBS-1 Bardet-Biedl syndrome, type 1 (BBS-1) 209900 - - - ARL6, BBS1, CCDC28B, MKS1, TMEM67 - -
04364 BBS-3 Bardet-Biedl syndrome, type 3 (BBS-3) 600151 - - - ARL6 - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
00888 RP-55 retinitis pigmentosa, type 55 (RP-55) 613575 - - - ARL6 - -
04048 SPG-61 paraplegia, spastic, type 61, autosomal recessive (SPG-61) 615685 - - - ARL6IP1 - -
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