A term referring to disorders characterized by abnormalities in the development of bones and cartilage. [ NCIT:C84978 ]
Synonyms: osteochondrodysplasia congenital skeletal dysplasia osteochondrodysplasia syndrome
Term information
- MESH:D010009 (MONDO:equivalentTo)
- NCIT:C84978 (MONDO:equivalentTo)
- EFO:0005571 (MONDO:equivalentTo)
- SCTID:105985007 (MONDO:equivalentTo)
- ICD9:756.4 (EFO:0005571)
- DOID:2256 (MONDO:equivalentTo)
- UMLS:C0029422 (NCIT:C84978)
http://identifiers.org/snomedct/105985007
http://purl.obolibrary.org/obo/NCIT_C84978
http://purl.obolibrary.org/obo/DOID_2256
http://linkedlifedata.com/resource/umls/id/C0029422
http://identifiers.org/mesh/D010009