bone and bones

Preferred Label : bone and bones;

MeSH definition : A specialized CONNECTIVE TISSUE that is the main constituent of the SKELETON. The principle cellular component of bone is comprised of OSTEOBLASTS; OSTEOCYTES; and OSTEOCLASTS, while FIBRILLAR COLLAGENS and hydroxyapatite crystals form the BONE MATRIX.; A specialized CONNECTIVE TISSUE that is the main constituent of the SKELETON. The principal cellular component of bone is comprised of OSTEOBLASTS; OSTEOCYTES; and OSTEOCLASTS, while FIBRILLAR COLLAGENS and hydroxyapatite crystals form the BONE MATRIX.;

MeSH synonym : bones and bone; bones and bone tissue; Bone and Bone;

DeCS synonym : Condyle;

MeSH hyponym : bone tissue; bones; Bone Tissues; Tissue, Bone; Tissues, Bone; Bony Apophyses; Apophyses, Bony; Bony Apophysis; Apophysis, Bony; Condyles; Bone;

MeSH annotation : /cytol: consider also OSTEOBLASTS; OSTEOCLASTS; OSTEOCYTES; /embryol: consider also OSTEOGENESIS; /surg: consider also OSTEOTOMY or ARTHRODESIS or FRACTURE FIXATION & its specifics; osteosynthesis not one of the preceding terms goes under BONE AND BONES /surg; differentiate from SKELETON which is almost never used: restrict SKELETON to bone arrangement as a whole & not for skeletal which usually means bone ( BONE AND BONES); disappearing bone OSTEOLYSIS, ESSENTIAL; inflammation OSTEITIS; necrosis OSTEONECROSIS; bone minerals BONE AND BONES (IM) MINERALS (IM) or specific mineral (IM); /cytol: consider also OSTEOBLASTS; OSTEOCLASTS; OSTEOCYTES; /embryol: consider also OSTEOGENESIS; /surg: consider also OSTEOTOMY or ARTHRODESIS or FRACTURE FIXATION & its specifics; differentiate from SKELETON which is almost never used: restrict SKELETON to bone arrangement as a whole & not for skeletal which usually means bone ( BONE AND BONES); inflammation OSTEITIS; necrosis OSTEONECROSIS;;

Wikipedia link : https://en.wikipedia.org/wiki/Bone;

Details

Origin ID

D001842;

UMLS CUI

C0005931;

Allowable qualifiers
- abnormalities [MeSH Qualifier]
- anatomy and histology [MeSH Qualifier]
- blood supply [MeSH Qualifier]
- chemistry [MeSH Qualifier]
- cytology [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- drug effects [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- immunology [MeSH Qualifier]
- injuries [MeSH Qualifier]
- innervation [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- radiation effects [MeSH Qualifier]
- surgery [MeSH Qualifier]
- ultrastructure [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Bin [NCIt concept]
- Bone [FMA entity]
- Bone [ICHI extension code]
- Bone [ICHI target]
- Bone [LOINC part]
- Bone [LOINC System]
- Bone [ICNP localization]
- Bone [LOINC System]
- Bone [NCIt concept]
- Bone (tissue) structure (body structure) [SNOMED CT concept]
- Bone Tissue [NCIt concept]
- Bone finding (finding) [SNOMED CT concept]
- Bone function (observable entity) [SNOMED CT concept]
- Bone organ [FMA entity]
- Bone part (body structure) [SNOMED CT concept]
- Bone structure of face (body structure) [SNOMED CT concept]
- Bone tissue [ICD-11 Extension code]
- Bone tissue [FMA entity]
- Bone tissue of long bone [FMA entity]
- Bone tissue structure of long bone (body structure) [SNOMED CT concept]
- Bones [PCS menu]
- Bones [ICD-11 Extension code]
- Bones [ICHI extension code]
- Bones [LOINC part]
- Bones [LOINC System]
- Bones [LOINC System]
- Cell of bone (cell) [SNOMED CT concept]
- Condyle [NCIt concept]
- Condyle [FMA entity]
- Disorder of bone (disorder) [SNOMED CT concept]
- Ectopic bone tissue (morphologic abnormality) [SNOMED CT concept]
- Entire bone organ (body structure) [SNOMED CT concept]
- Entire bony skeleton (body structure) [SNOMED CT concept]
- Facial bones [LOINC System]
- Left eye [FMA entity]
- Operating System [NCIt concept]
- Opitz gbbb syndrome [OMIM Phenotype]
- Osseous metaplasia (morphologic abnormality) [SNOMED CT concept]
- Osteopetrosis [ICD-10 Sub-category (who)]
- Other congenital malformations of lower limb(s), including pelvic girdle [ICD-10 Sub-category (who)]
- Other congenital malformations of musculoskeletal system [ICD-10 Sub-category (who)]
- Other congenital malformations of upper limb(s), including shoulder girdle [ICD-10 Sub-category (who)]
- Other specified congenital malformations of skull and face bones [ICD-10 Sub-category (who)]
- Set of bone organs [FMA entity]
- Skeletal system structure (body structure) [SNOMED CT concept]
- Structure of condyle (body structure) [SNOMED CT concept]
- bone [ICHI extension code]
- bone organ [Radlex concept]
- bone tissue [UBERON concept]
- bone, nos [SNOMED Notion]
- bones [ICF N3 Element]
- bones of face [ICF N3 Element]
- bony tissue, nos [SNOMED Notion]
- condyle [Radlex concept]
- condyle [UBERON concept]
- long bone [Radlex concept]
- long bone [SNOMED Notion]
- part of bone [Radlex concept]
- set of bone organs [Radlex concept]
- skeletal system, nos [SNOMED Notion]
Indexing information
- bone ash [MeSH Supplementary Concept]
- bone meal [MeSH Supplementary Concept]
- matrigenin [MeSH Supplementary Concept]
- matrix gla protein [MeSH Supplementary Concept]
- phosphoprotein 66 kDa, rat [MeSH Supplementary Concept]
- true bone ceramics [MeSH Supplementary Concept]
Record concept(s)
- Condyle [MeSH concept]
- bone and bones [MeSH concept]
- bone tissue [MeSH concept]
- bones [MeSH concept]
Related MeSH Supplementary Concept(s)
- Al-Gazali syndrome [MeSH Supplementary Concept]
- Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities [MeSH Supplementary Concept]
- SCARF syndrome [MeSH Supplementary Concept]
- Verloove-Vanhorick brubakk syndrome [MeSH Supplementary Concept]
- arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly [MeSH Supplementary Concept]
- asymmetric short stature syndrome [MeSH Supplementary Concept]
- baby rattle pelvic dysplasia [MeSH Supplementary Concept]
- beemer ertbruggen syndrome [MeSH Supplementary Concept]
- bone fragility with contractures, arterial rupture, and deafness [MeSH Supplementary Concept]
- chitty hall webb syndrome [MeSH Supplementary Concept]
- circumvallate placenta syndrome [MeSH Supplementary Concept]
- cranioectodermal dysplasia [MeSH Supplementary Concept]
- creases, Infra-Auricular cutaneous, with tall stature and advanced bone age [MeSH Supplementary Concept]
- dembone [MeSH Supplementary Concept]
- dentin dysplasia sclerotic bones [MeSH Supplementary Concept]
- expansile bone lesions [MeSH Supplementary Concept]
- faciocardiomelic syndrome [MeSH Supplementary Concept]
- flat umbilicus familial [MeSH Supplementary Concept]
- hutterite cerebroosteonephrodysplasia syndrome [MeSH Supplementary Concept]
- hypochondroplasia [MeSH Supplementary Concept]
- iridogoniodysgenesis and skeletal anomalies [MeSH Supplementary Concept]
- kozlowski brown hardwick syndrome [MeSH Supplementary Concept]
- kozlowski ouvrier syndrome [MeSH Supplementary Concept]
- lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones [MeSH Supplementary Concept]
- lubboc [MeSH Supplementary Concept]
- microcephaly seizures mental retardation heart disorders [MeSH Supplementary Concept]
- microcephaly, severe, with skeletal anomalies including posterior Rib-Gap defects [MeSH Supplementary Concept]
- myopathy, limb-girdle, with bone fragility [MeSH Supplementary Concept]
- myotonia with skeletal abnormalities and mental retardation [MeSH Supplementary Concept]
- osteomen [MeSH Supplementary Concept]
- pena shokeir syndrome type 2 [MeSH Supplementary Concept]
- pseudohermaphroditism, female, with skeletal anomalies [MeSH Supplementary Concept]
- pyrost [MeSH Supplementary Concept]
- satoyoshi syndrome [MeSH Supplementary Concept]
- short limb dwarfism al gazali type [MeSH Supplementary Concept]
- silengo lerone pelizza syndrome [MeSH Supplementary Concept]
- slavotinek pike mills hurst syndrome [MeSH Supplementary Concept]
- spastic paraplegia 9, autosomal dominant [MeSH Supplementary Concept]
- theodor hertz goodman syndrome [MeSH Supplementary Concept]
- van den bosch syndrome [MeSH Supplementary Concept]
Related MeSH term(s)
- bone development [MeSH Descriptor]
- bone transplantation [MeSH Descriptor]
See also
- arthrodesis [MeSH Descriptor]
- calcification, physiologic [MeSH Descriptor]
- osteogenesis [MeSH Descriptor]
- osteotomy [MeSH Descriptor]
- skeleton [MeSH Descriptor]
See also (suggested by CISMeF)
- bone demineralization technique [MeSH Descriptor]
- bone development [MeSH Descriptor]
- bone diseases [MeSH Descriptor]
- bone lengthening [MeSH Descriptor]
- bone remodeling [MeSH Descriptor]
- bone substitutes [MeSH Descriptor]
- bone transplantation [MeSH Descriptor]
- fracture healing [MeSH Descriptor]
- fractures, bone [MeSH Descriptor]
- infusions, intraosseous [MeSH Descriptor]
- osteology [MeSH Descriptor]
Semantic type(s)
- Tissue [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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