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osteochondrodysplasia

^ http://purl.obolibrary.org/obo/MONDO_0005516

A term referring to disorders characterized by abnormalities in the development of bones and cartilage. [ NCIT:C84978 ]

Term info

database cross reference
  • ICD9:756.4 (EFO:0005571)
  • EFO:0005571 (MONDO:equivalentTo)
  • GARD:0006051 (MONDO:shared-umls-xref)
  • DOID:2256 (MONDO:equivalentTo)
  • SCTID:105985007 (MONDO:equivalentTo)
  • UMLS:C0029422 (NCIT:C84978)
  • MESH:D010009 (MONDO:equivalentTo)
  • NCIT:C84978 (MONDO:equivalentTo)
definition

A term referring to disorders characterized by abnormalities in the development of bones and cartilage.

exactMatch

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

has exact synonym

osteochondrodysplasia, congenital skeletal dysplasia, osteochondrodysplasia syndrome

has narrow synonym

congenital anomaly of cartilage, cartilage development disorder

has related synonym

skeletal dysplasia

id

MONDO:0005516