All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
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 - -
01095 ISQMR Ichthyosis, spastic quadriplegia, and mental retardation 614457 AR - - ELOVL4 - -
01323 SCA34 Spinocerebellar ataxia 34 133190 AD - - ELOVL4 - -
01094 STGD3 Macular dystrophy, autosomal dominant, chromosome 6-linked (Stargardt disease, type 3 (STGD-3)) 600110 AD - - ELOVL4 - -
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