Disease table of PONTOCEREBELLAR HYPOPLASIA, TYPE 1C OMIM ID: 616081

Gene-disease associations table

GeneAssociated with PONTOCEREBELLAR HYPOPLASIA, TYPE 1C inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
EXOSC8ClinVar, OMIM, HUMSAVARHGNC link13q13.31616081

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