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 - -
02477 MLC leukoencephalopathy, megalencephalic, with subcortical cysts (MLC) - - 625 607 HEPACAM, MLC1 - -
00805 MLC2A leukoencephalopathy, megalencephalic, with subcortical cysts, type 2A (MLC2A) 613925 AR - - HEPACAM - -
00806 MLC2B leukoencephalopathy, megalencephalic with subcortical cysts 2B, remitting, with/without mental retardation, type 2B (MLC2B) 613926 AD - - HEPACAM - -
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