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Summary Literature (0)
MIM:613076 - MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT AND DEVELOPMENTAL DELAY; MPMCD

Xenbase Genes: gfer

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013116 - congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome