Summary Literature (0)

MIM:611091 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5; MRT5

Echinobase Genes: nsun2

Human Disease Resource: OMIM


Disease Ontology (DO):

DOID:0060308 - autosomal recessive non-syndromic intellectual disability

DOID:0081181 - autosomal recessive intellectual developmental disorder 5