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
05599 CAMRQ ataxia, cerebellar, mental retardation, quadrupedal locomotion (CAMRQ) - - 14 14 ATP8A2, CA8, VLDLR, WDR81 - -
01096 CAMRQ3 ataxia, cerebellar, and mental retardation with/without quadrupedal locomotion, type 3 (CAMRQ-3) 613227 AR 1 1 CA8 - autosomal recessive
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 - -
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