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

Synonyms: osteochondrodysplasia congenital skeletal dysplasia osteochondrodysplasia syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:10495 (MONDO:equivalentTo)
  • UMLS:C0029422 (MONDO:equivalentTo)
  • NCIT:C84978 (MONDO:equivalentTo)
  • DOID:2256 (MONDO:equivalentTo)
  • MESH:D010009 (MONDO:equivalentTo)
  • ICD9:756.4 (EFO:0005571)
  • SCTID:105985007 (MONDO:equivalentTo)
  • EFO:0005571 (MONDO:equivalentTo)
Subsets

otar

exactMatch

http://purl.obolibrary.org/obo/NCIT_C84978

http://identifiers.org/medgen/10495

http://identifiers.org/snomedct/105985007

http://purl.obolibrary.org/obo/DOID_2256

http://linkedlifedata.com/resource/umls/id/C0029422

http://identifiers.org/mesh/D010009

has narrow synonym

congenital anomaly of cartilage

cartilage development disorder

has related synonym

skeletal dysplasia

id

MONDO:0005516