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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: OMIM


Disease Ontology (DO):
DOID:0050888 - syndromic intellectual disability
DOID:0080311 - X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance