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Summary Literature (0)
MIM:617468 - ARTHROGRYPOSIS MULTIPLEX CONGENITA 1, NEUROGENIC, WITH MYELIN DEFECT; AMC1

Xenbase Genes: lgi4

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008823 - arthrogryposis multiplex congenita 2, neurogenic type
MONDO:0060486 - arthrogryposis multiplex congenita 1, neurogenic, with myelin defect

Disease Ontology (DO):
DOID:0080978 - arthrogryposis multiplex congenita-1