Summary Literature (0)

MIM:615637 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41

Echinobase Genes: kptn

Human Disease Resource: OMIM


Disease Ontology (DO):

DOID:0060308 - autosomal recessive non-syndromic intellectual disability

DOID:0081206 - autosomal recessive intellectual developmental disorder 41