272673000: Bone structure (body structure)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Bone structure	Is a	Body organ structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Bone structure	Is a	Bone and/or joint structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Bone structure	partie de	Entire body as a whole (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Bone structure	Is a	Skeletal system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Bone structure	partie de	Entire musculoskeletal system	false	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Bone structure	Is a	Connective tissue structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Bone structure	Is a	Structure of bone organ	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Bone structure	Is a	Bony skeleton subdivision	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Juvenile osteochondrosis of hand (disorder)	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Osteophyte of left knee (disorder)	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Heberden node of the distal interphalangeal joints of the left hand	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Bilateral osteophyte of knees	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Heberden node (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Right Heberdens nodes with arthropathy	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sporotrichosis of the bones	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
X-linked osteoporosis with fractures	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly, short stature, retinitis pigmentosa syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Chondrodysplasia with joint dislocations gPAPP type (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder)	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spondyloepimetaphyseal dysplasia Isidor type	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
High bone mass osteogenesis imperfecta	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Spondylometaphyseal dysplasia A4 type (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
X-linked calvarial hyperostosis	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Dysplasie, spondyloepimetaphysäre, Typ Czarny-Ratajczak	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Richieri Costa-da Silva syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Infection of bone associated with bone fixation device (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Infected plate or screw	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Infection of internal Kirschner wire fixator	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pelvic dysplasia, arthrogryposis of lower limbs syndrome (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Infection of bone associated with bone wire (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
An extremely rare primary bone dysplasia with increased bone density with characteristics of lethal neonatal dwarfism with hydrops, narrow chest and short limbs with extensive cortical thickening of all long bones, ribs, clavicles and scapulae and coronal clefts in vertebral bodies.	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Infection of bone associated with external fixator pin	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Radial deficiency, tibial hypoplasia syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Infection of bone associated with intramedullary rod	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Stickler syndrome type 3 (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteomesopycnosis	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Osteosclerosis	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A primary bone dysplasia disorder that encompasses a group of congenital anomalies that are characterized by skeletal dysplasia of varying clinical severity and an X linked dominant pattern of inheritance. This group includes otopalatodigital syndrome type 1 and 2 (OPD1, OPD2) which are characterized in affected males by cleft palate, conductive hearing loss, craniofacial abnormalities and skeletal dysplasia; Melnick-Needles syndrome (MNS) which displays skeletal deformities in females and embryonic or perinatal lethality in most males; frontometaphyseal dysplasia (FMD); and terminal osseous dysplasia - pigmentary defects.	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Secondary non-traumatic avascular necrosis of bone	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteopathia striata, pigmentary dermopathy, white forelock syndrome (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Bowing deformity of bone	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mixed sclerosing bone dystrophy with extra-skeletal manifestation	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Infection of bone associated with spinal fixation device	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal recessive brachyolmia (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare genetic bone development disorder characterized by occipital and parietal bone hypoplasia leading to occipital encephalocele, calvarial mineralization defects, craniosynostosis, radiohumeral fusions, oligodactyly and other skeletal anomalies (arachnodactyly, terminal phalangeal aplasia of the thumbs, bilateral absence of the great toes, pronounced bilateral angulation of femora, shortened limbs, advanced osseous maturation). Fetal death in utero is associated. There is evidence the disease can be caused by homozygous mutation in the CYP26B1 gene on chromosome 2p13.	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal recessive cutis laxa type 2A	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Dysplasia with increased bone density	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Brachydactylous dwarfism Mseleni type	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Menkes kinky-hair syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Mixed sclerosing bone dysplasia (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Spondylometaphyseal dysplasia, bowed forearms, facial dysmorphism syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Syndactyly, polydactyly, ear lobe syndrome (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare genetic disease characterised by mild intellectual disability, osteoporosis, delayed bone age, macrocephaly with wormian bones and frontal bossing, anomalies of fingers, nails, and teeth, thoracic deformities, hyperextensibility of joints, as well as congenital amaurosis and paraplegia. There have been no further descriptions in the literature since 1981.	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Gonococcal osteomyelitis (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Schwartz-Jampel syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hypophosphatemic rickets with nephrotic-glycosuric dwarfism	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Autosomal dominant hypophosphatemic rickets	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Autosomal dominant hypophosphatemic bone disease	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Axial osteosclerosis	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Francois syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Aluminium bone disease	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Aluminum-related osteomalacia (disorder)	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fracture of bone due to accidental fall	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Reduced ossification (finding)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Division and displacement of bone (procedure)	Procedure site - Direct (attribute)	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Neonatal osteosclerotic dysplasia (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Blomstrand dysplasia (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Raine dysplasia (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Q fever osteomyelitis (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Osteomyelitis	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
SAPHO syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Bacterial osteomyelitis	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Seckel syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Klippel-Feil sequence (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Salmonella osteomyelitis	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Desmosterolosis (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Potocki-Shaffer syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hemangioma of bone (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
ostéomyélite chronique à cellules plasmatiques symétriques	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Ossification anomaly with psychomotor developmental delay syndrome	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Wildervanck syndrome (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial x-linked hypophosphatemic vitamin D refractory rickets	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Osteitis fibrosa cystica	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Osteomyelitis of multiple sites	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fracture of multiple bones	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Erosion of bone	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fracture of bone after implantation of orthopedic device (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
An extremely rare type of severe combined immunodeficiency syndrome (SCID) characterized by the classical signs of T-B- SCID (severe and recurrent infections, diarrhea, failure to thrive, absence of T and B lymphocytes) associated with skeletal anomalies like short stature, bowing of the long bones and metaphyseal abnormalities of variable degree of severity.	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteomyelitis due to type 1 diabetes mellitus (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Osteomyelitis due to type 2 diabetes mellitus	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Injection of bone using computed tomography guidance (procedure)	Procedure site - Indirect (attribute)	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Injection of bone using computed tomography guidance (procedure)	Procedure site - Direct (attribute)	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
CT guided aspiration of bone	Procedure site - Indirect (attribute)	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
CT guided aspiration of bone	Procedure site - Direct (attribute)	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Entire bony bone	Is a	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)
Malignant neoplasm of bone, connective tissue, skin and breast (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Carcinoma of bone, connective tissue, skin and breast (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Autosomal dominant hypophosphatemic rickets	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal dominant hypophosphatemic bone disease	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Radiotherapy to bone	Procedure site - Direct (attribute)	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Chondrodysplasia punctata due to maternal autoimmune disease (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
pathologie rénale chronique associée à une ostéoporose	Finding site	False	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Renal osteodystrophy with high bone turnover	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Renal osteodystrophy with normal bone turnover (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Renal osteodystrophy with low bone turnover (disorder)	Finding site	True	Bone structure	Inferred relationship	Existential restriction modifier (core metadata concept)	1

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
407865012	Bone structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
665231017	Bone structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
407865012	Bone structure	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
407865012	Bone structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
665231017	Bone structure (body structure)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
665231017	Bone structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
275241000077116	structure osseuse	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
925831000172115	ossa	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
992971000172114	os	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
275241000077116	structure osseuse	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
925831000172115	ossa	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
992971000172114	os	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module