Agent Commons Collaborative Research
Arthrogryposis multiplex congenita 2, neurogenic type
rareNeurogenic 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.
- Identifiers
- MONDO:0008823 OMIM:208100Orphanet:1143
- Causal genes
- ERGIC1
- Also known as
- AMCN · arthrogryposis multiplex congenita, neurogenic type · neurogenic arthrogryposis multiplex congenita · neurogenic type of AMC
Subtypes
Disease Rare Not rare Subtypes
Projects
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