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 - -
01068 MNK Menkes disease 309400 XLR 339 339 ATP7A - -
01069 OHS occipital horn syndrome (OHS) 304150 XLR 15 15 ATP7A - -
01070 SMAX3 atrophy, muscular, spinal, distal, X-linked, type 3 (SMAX3) 300489 XLR - - ATP7A - -
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