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)) - - 23 23 ELP2, LINGO1, MBOAT7, METTL5, PGAP1 - autosomal recessive
04087 MRT42;GPIBD9 mental retardation, autosomal recessive, type 42 (MRT-42, glycosylphosphatidylinositol deficiency, type 9 (GPIBD-9)) 615802 AR 3 3 PGAP1 - autosomal recessive
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