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Summary Literature (0)
MIM:208100 - ARTHROGRYPOSIS MULTIPLEX CONGENITA 2, NEUROGENIC TYPE; AMC2

Xenbase Genes: ergic1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008823 - arthrogryposis multiplex congenita 2, neurogenic type

Disease Ontology (DO):
DOID:0090124 - neurogenic-type arthrogryposis multiplex congenita-2