All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05532 MRD mental retardation, autosomal dominant (MRD, intellectual disability (IDD)) - - 12 12 CAMK2A, CIC, CTCF, KCNQ5, NUS1 - autosomal dominant
05884 MRD45 mental retardation, autosomal dominant, type 45 (MRD45) 617600 AD 2 2 CIC - -
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