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
04147 MRT mental retardation, autosomal recessive (MRT, intellectual disability (IDT)) - - 24 24 ELP2, LINGO1, LINS, MBOAT7, METTL5, PGAP1 - autosomal recessive
05948 MRT58 mental retardation, autosomal recessive, type 58 (MRT58) 617270 AR - - ELP2 - -
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