Disease table of MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE OMIM ID: 300486

Gene-disease associations table

GeneAssociated with MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
OPHN1ClinVar, OMIMHGNC linkXq121300486

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