arthrogryposis, distal, with mental retardation and characteristic facies

Preferred Label : arthrogryposis, distal, with mental retardation and characteristic facies;

Origin ID

C565940;

UMLS CUI

C1859723;

Automatic exact mappings (from CISMeF team)
- Arthrogryposis, distal, with impaired intellectual development and characteristic facies [OMIM Phenotype]
MeSH term(s) associated for indexing
- arthrogryposis [MeSH Descriptor]
- facies [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
Record concept(s)
- arthrogryposis, distal, with mental retardation and characteristic facies [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Arthrogryposis, distal, with impaired intellectual development and characteristic facies [OMIM Phenotype]