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Summary Literature (0)
MIM:601553 - HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD

Xenbase Genes: cdh3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011107 - synovial joint of pelvic girdle

Disease Ontology (DO):
DOID:0110711 - congenital hypotrichosis with juvenile macular dystrophy