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
05533 MR;ID mental retardation (MR, intellectual disability (ID)) - - 53 50 CAMK2A, CLTC, DLG4, GRIA1, NONO - -
05532 MRD mental retardation, autosomal dominant (MRD, intellectual disability (IDD)) - - 12 12 CAMK2A, CIC, CTCF, KCNQ5, NUS1 - autosomal dominant
05938 MRD53 mental retardation, autosomal dominant, type 53 (MRD53) 617798 AD 2 1 CAMK2A - -
06670 MRT63 ?Mental retardation, autosomal recessive 63 618095 AR - - CAMK2A - -
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