MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42

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Echinobase

Summary

Literature (0)

MIM:615802 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42

Echinobase Genes: pgap1

Human Disease Resource: OMIM

Disease Ontology (DO):

DOID:0060308 - autosomal recessive non-syndromic intellectual disability

DOID:0060308 - autosomal recessive non-syndromic intellectual disability