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
03660 CCHLND cataracts, congenital, hearing loss, and neurodegeneration (CCHLND) 614482 - 1 0 SLC33A1 - -
00139 ID intellectual disability (ID) - - 1837 1570 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 536 more - -
03149 SPG-42 paraplegia, spastic, type 42, autosomal dominant (SPG-42) 612539 - 1 0 SLC33A1 - -
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