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
04495 EIEE-27 encephalopathy, epileptic, early infantile, type 27 (EIEE-27) 616139 - 0 0 GRIN2B - -
01889 FESD epilepsy, focal, with speech disorder with or without mental retardation (FESD) 245570 - 1 1 GRIN2A - -
03242 MACS MACS syndrome (MACS, macrocephaly, alopecia, cutis laxa, and scoliosis) 613075 - 2 2 RIN2 - -
00807 MRD-6 mental retardation, autosomal dominant, type 6 (MRD-6) 613970 - 2 2 GRIN2B - -
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