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
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 - -
05153 MCPH microcephaly, primary, autosomal recessive (MCPH) - - 8 8 CEP152, MCPH1, MFSD2A, WDFY3 - -
00393 MCPH1 microcephaly, type 1, primary, autosomal recessive (MCPH-1) 251200 AR 5 5 MCPH1 - -
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