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