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Summary Literature (0)
MIM:616875 - CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR

Xenbase Genes: emc1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014811 - cerebellar atrophy, visual impairment, and psychomotor retardation;

Disease Ontology (DO):
DOID:0081276 - cerebellar atrophy, visual impairment, and psychomotor retardation