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Summary Literature (0)
MIM:265000 - MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS

Xenbase Genes: chrng

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009926 - autosomal recessive multiple pterygium syndrome

Disease Ontology (DO):
DOID:0080110 - contractures, pterygia, and spondylocarpotarsal fusion syndrome