osteochondrodysplasia

Term ID

DOID:2256

Synonyms

Cartilage Development disorder
chondrodystrophy
Congenital anomaly of cartilage
Osteochondrodysplasia syndrome
skeletal dysplasia

Definition

A bone development disease that results_in defective development of cartilage or bone. http://en.wikipedia.org/wiki/Osteochondrodysplasia

References

ICD10CM:Q78.9
ICD9CM:756.4
MESH:D010009
NCI:C34466
NCI:C84978
SNOMEDCT_US_2023_03_01:205510001
SNOMEDCT_US_2023_03_01:67988000
UMLS_CUI:C0008449
UMLS_CUI:C0029422

Ontology

Human Disease ( DOID:2256 )

Relationships

is a type of: bone development disease cartilage disease

bone development disease cartilage disease Show first 5 Terms
has subtype: acheiropody achondrogenesis achondroplasia acrocapitofemoral dysplasia acromesomelic dysplasia ... Show All 52 Terms

acheiropody achondrogenesis achondroplasia acrocapitofemoral dysplasia acromesomelic dysplasia acromicric dysplasia atelosteogenesis Blount's disease Boomerang dysplasia brachyolmia calvarial doughnut lesions with bone fragility campomelic dysplasia chondrodysplasia Blomstrand type chondrodysplasia with joint dislocations gPAPP type cleidocranial dysplasia Desbuquois dysplasia diaphyseal medullary stenosis with malignant fibrous histiocytoma diastrophic dysplasia fibrochondrogenesis gnathodiaphyseal dysplasia hypertrichotic osteochondrodysplasia Cantu type hypochondrogenesis hypochondroplasia Kenny-Caffey syndrome Kniest dysplasia Leri-Weill dyschondrosteosis metachondromatosis metaphyseal dysplasia metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly, short stature, and limb abnormalities midface dysplasia multiple epiphyseal dysplasia omodysplasia osteogenesis imperfecta osteoglophonic dysplasia otospondylomegaepiphyseal dysplasia, autosomal dominant otospondylomegaepiphyseal dysplasia, autosomal recessive parastremmatic dwarfism progressive pseudorheumatoid arthropathy of childhood pseudoachondroplasia pycnodysostosis schneckenbecken dysplasia Silverman-Handmaker type dyssegmental dysplasia spondyloepimetaphyseal dysplasia spondyloepiphyseal dysplasia spondylometaphyseal dysplasia spondyloperipheral dysplasia thanatophoric dysplasia Torrance type platyspondylic dysplasia Weissenbacher-Zweymuller syndrome Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models