arthrogryposis multiplex congenita neurogenic type

Preferred Label : arthrogryposis multiplex congenita neurogenic type;

MeSH synonym : neurogenic type of AMC; AMC, neurogenic type; arthrogryposis multiplex congenita, neurogenic type;

Details

Origin ID

C536614;

UMLS CUI

C1859721;

CISMeF manual mappings
- Neurogenic arthrogryposis multiplex congenita [ORDO Disease]
Currated CISMeF NLP mapping
- Neurogenic arthrogryposis multiplex congenita (disorder) [SNOMED CT concept]
- neurogenic-type arthrogryposis multiplex congenita-2 [DO Concept]
DO Cross reference
- neurogenic-type arthrogryposis multiplex congenita-2 [DO Concept]
MeSH term(s) associated for indexing
- arthrogryposis [MeSH Descriptor]
ORDO relation(s)
- Neurogenic arthrogryposis multiplex congenita [ORDO Disease]
Record concept(s)
- Arthrogryposis multiplex congenita neurogenic type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Arthrogryposis multiplex congenita 2, neurogenic type [OMIM Phenotype]
- Neurogenic arthrogryposis multiplex congenita [ORDO Disease]
- Neurogenic arthrogryposis multiplex congenita (disorder) [SNOMED CT concept]
- neurogenic-type arthrogryposis multiplex congenita-2 [DO Concept]
Validated automatic mappings to BTNT
- Arthrogryposis multiplex congenita 2, neurogenic type [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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