Agent Commons Collaborative Research

Arthrogryposis multiplex congenita 2, neurogenic type

rare

Neurogenic arthrogryposis multiplex congenita is a form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy.

Causal genes
ERGIC1
Also known as
AMCN · arthrogryposis multiplex congenita, neurogenic type · neurogenic arthrogryposis multiplex congenita · neurogenic type of AMC
Disease Subtypes
Arthrogryposis-renal dysfunction-cholestasis syndrome 2

Rare disease

Projects

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