Smith-McCort dysplasia

Preferred Label : Smith-McCort dysplasia;

MeSH note : mutation in DYM;

Origin ID

C564589;

UMLS CUI

C1846431;

Automatic exact mappings (from CISMeF team)
- Smith-mccort dysplasia [OMIM phenotypic series]
Currated CISMeF NLP mapping
- Smith McCort dysplasia (disorder) [SNOMED CT concept]
- Smith-McCort dysplasia [DO Concept]
- Smith-McCort dysplasia [ICD-11 More detail]
- Smith-McCort dysplasia [ORDO Disease]
- Smith-mccort dysplasia 1 [OMIM Phenotype]
- Smith-mccort dysplasia 2 [OMIM Phenotype]
DO Cross reference
- Smith-McCort dysplasia [DO Concept]
MeSH term(s) associated for indexing
- osteochondrodysplasias [MeSH Descriptor]
Record concept(s)
- Smith-McCort dysplasia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Smith McCort dysplasia (disorder) [SNOMED CT concept]
- Smith-McCort dysplasia [ORDO Disease]
- Smith-McCort dysplasia [DO Concept]