arthrogryposis multiplex congenita 2, neurogenic type
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. [ Orphanet:1143 ]
Term info
- DOID:0090124 (MONDO:equivalentTo)
- GARD:0000790 (MONDO:equivalentTo)
- SCTID:715316005 (MONDO:equivalentTo)
- UMLS:C1859721 (Orphanet:1143/e)
- OMIM:208100 (Orphanet:1143/e)
- Orphanet:1143 (OMIM:208100)
- MESH:C536614 (Orphanet:1143/e)
ordo_disease
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.
http://identifiers.org/mesh/C536614, http://linkedlifedata.com/resource/umls/id/C1859721, http://identifiers.org/snomedct/715316005, https://omim.org/entry/208100, http://purl.obolibrary.org/obo/DOID_0090124, http://purl.obolibrary.org/obo/Orphanet_1143
AMCN, AMC neurogenic type, arthrogryposis multiplex congenita neurogenic type, neurogenic arthrogryposis multiplex congenita
neurogenic type of AMC, AMC, neurogenic type, arthrogryposis multiplex congenita, neurogenic type
MONDO:0008823