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Summary Literature (0)
MIM:616819 - CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA

Xenbase Genes: frmd4a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014787 - severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome