MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE

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Echinobase

Summary

Literature (0)

MIM:300486 - MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE

Echinobase Genes:

Human Disease Resource: MIM

Disease Ontology (DO):

DOID:0050888 - syndromic intellectual disability
DOID:0080311 - X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance

DOID:0050888 - syndromic intellectual disability

DOID:0080311 - X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance