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
04087 NEDDSBA;MRT42;GPIBD9 neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities (MRT-42, GPIBD-9) 615802 AR 3 3 PGAP1 - autosomal recessive
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