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arthrogryposis multiplex congenita 2, neurogenic type

Go to external page http://purl.obolibrary.org/obo/MONDO_0008823

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 ]

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

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:1143 (OMIM:208100)
  • UMLS:C5435650 (MONDO:equivalentTo)
  • OMIM:208100 (Orphanet:1143/e)
  • GARD:790 (Orphanet:1143)
  • SCTID:715316005 (MONDO:equivalentTo)
  • MESH:C536614 (Orphanet:1143/e)
  • DOID:0090124 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare

exactMatch

http://identifiers.org/mesh/C536614

http://identifiers.org/snomedct/715316005

http://www.orpha.net/ORDO/Orphanet_1143

https://omim.org/entry/208100

http://purl.obolibrary.org/obo/DOID_0090124

http://linkedlifedata.com/resource/umls/id/C5435650

has related synonym

neurogenic type of AMC

AMC, neurogenic type

arthrogryposis multiplex congenita, neurogenic type

id

MONDO:0008823

Term relations