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Echinobase
Summary Literature (0)
DOID:0090124 - neurogenic arthrogryposis multiplex congenita

Disease Ontology Definition:A nervous system disease characterized by congenital contractures at the elbows and knees, myopathy, absence of muscle spindles, congenital heart disease and spinal motor nueron depletion that has_material_basis_in variation in the chromosome region 5q35.

Synonyms: AMC neurogenic type, AMCN, arthrogryposis multiplex congenita neurogenic type,

Echinobase Genes :



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): nervous system disease (is_a)