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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:

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
3318101000005115 Knoglestruktur da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


4776 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Bone structure Is a An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary). false Inferred relationship Some
Bone structure Is a Bone and/or joint structure (body structure) true Inferred relationship Some
Bone structure del af Entire body as a whole false Inferred relationship Some
Bone structure Is a Skeletal system structure false Inferred relationship Some
Bone structure del af Entire musculoskeletal system false Additional relationship Some
Bone structure Is a Connective tissue structure false Inferred relationship Some
Bone structure Is a Structure of bone organ true Inferred relationship Some
Bone structure Is a Bony skeleton subdivision true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Ehlers-Danlos' syndrom, recessiv type 4 Finding site False Bone structure Inferred relationship Some 1
Anden specificeret terapeutisk punktur af knogle Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Ostitis deformans associeret med anden sygdom Finding site False Bone structure Inferred relationship Some 1
Hypoplastic chondrodystrophy Finding site True Bone structure Inferred relationship Some 1
Anden åben fraktursubluksation Finding site False Bone structure Inferred relationship Some 1
Bone shortening procedure Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Traction lengthening of diaphysis of bone Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 2
Spondylometaphyseal dysplasia - Sutcliffe type Finding site False Bone structure Inferred relationship Some 1
Congenital cerebral meningocele Finding site False Bone structure Inferred relationship Some 4
Knoglefraktur, uspecificeret Finding site False Bone structure Inferred relationship Some 1
Osteodysplasi Finding site False Bone structure Inferred relationship Some 1
Stickler syndrome Finding site False Bone structure Inferred relationship Some 1
Application of Steinmann pin traction Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Change of external fixator pin Procedure site - Indirect (attribute) True Bone structure Inferred relationship Some 1
Lethal retarded ossification syndromes Finding site False Bone structure Inferred relationship Some 1
Osteogenesis imperfecta type I (disorder) Finding site True Bone structure Inferred relationship Some 1
Intern fiksering af osteotomi, ikke klassificeret andetsteds Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Articulated prosthetic replacement of bone Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
A very rare lysosomal storage disease with characteristics of developmental delay of varying severity and hearing loss, but that can manifest a wide phenotypic heterogeneity. Finding site False Bone structure Inferred relationship Some 1
Filling of segmental defect by compression-distraction Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Osteogenesis imperfecta, type IV A Finding site False Bone structure Inferred relationship Some 1
Application of external fixator system Procedure site - Indirect (attribute) False Bone structure Inferred relationship Some 1
Attention to electromagnetic stimulator in bone Procedure site - Indirect (attribute) True Bone structure Inferred relationship Some 1
Tuberkuløs ostit med multiple cyster Finding site False Bone structure Inferred relationship Some 1
Application of external electromagnetic bone stimulator Procedure site - Indirect (attribute) True Bone structure Inferred relationship Some 1
Ehlers-Danlos' syndrom, ikke-hydroxylysinfattig okulær type Finding site False Bone structure Inferred relationship Some 1
Progressive pseudorheumatoid dysplasia Finding site False Bone structure Inferred relationship Some 1
Acromesomelic dysplasia Hunter-Thompson type (disorder) Finding site True Bone structure Inferred relationship Some 1
Filling of bone defect with bone cement Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
luksation eller subluksation, ikke nærmere specificeret Finding site False Bone structure Inferred relationship Some 2
Internal fixation of bone without fracture reduction Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Chondrodysplasia punctata Finding site False Bone structure Inferred relationship Some 1
Juvenile fucosidosis (disorder) Finding site False Bone structure Inferred relationship Some 1
Application of bone xenograft Procedure site - Indirect (attribute) False Bone structure Inferred relationship Some 1
Brachydactyly syndrome type B (disorder) Finding site False Bone structure Inferred relationship Some 1
Closed fracture subluxation of pelvis Finding site False Bone structure Inferred relationship Some 2
Short rib polydactyly syndrome Finding site False Bone structure Inferred relationship Some 1
Carcinoma of upper limb bones/scapula Finding site False Bone structure Inferred relationship Some 2
Yunis-Varon dysplasia (disorder) Finding site True Bone structure Inferred relationship Some 1
Open biopsy of lesion of bone Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 2
Obliteration of tympanomastoid cavity Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Revision to skeletal traction of fracture Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Chondrodysplasia punctata, MT type Finding site False Bone structure Inferred relationship Some 1
Trocar biopsy of bone Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Chondrodysplasia Finding site False Bone structure Inferred relationship Some 1
Terapeutisk punktur af knogle, ikke nærmere specificeret Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Hydromeningocele Finding site False Bone structure Inferred relationship Some 1
Åben tilsigtet frakturering, angulær korrektion og ekstern fiksering, uanset yderligere specifikation Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Canine hypertrophic osteodystrophy Finding site False Bone structure Inferred relationship Some 1
Excision af knogle, ikke nærmere specificeret Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Lenz-Majewski hyperostosis syndrome Finding site False Bone structure Inferred relationship Some 1
Fiksering af knogle, traktion, ikke nærmere specificeret Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 2
An autosomal recessive lysosomal storage disease belonging to the oligosaccharidosis group. Clinical signs include slowly developing intellectual disability beginning with clumsiness, late speech, and hyperkinesia, mild facial dysmorphism, and slight kyphoscoliosis. Caused by mutations in gene AGU located on 4q34.3. Transmission is autosomal recessive. Finding site False Bone structure Inferred relationship Some 1
Percutaneous diagnostic puncture of bone Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Spondyloepimetaphyseal disorder Finding site False Bone structure Inferred relationship Some 1
Migratory osteolysis Finding site True Bone structure Inferred relationship Some 1
kongenit chondrodysplasia punctata Finding site False Bone structure Inferred relationship Some 1
Anden lukket fraktursubluksation Finding site False Bone structure Inferred relationship Some 1
Reduction of open fracture with uncomplicated soft tissue closure Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
I-cell disease Finding site False Bone structure Inferred relationship Some 1
Fistulectomy of bone Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Osteogenesis imperfecta type III (disorder) Finding site True Bone structure Inferred relationship Some 1
Schneckenbecken dysplasia Finding site False Bone structure Inferred relationship Some 1
Adjustment of electromagnetic bone stimulator Procedure site - Indirect (attribute) True Bone structure Inferred relationship Some 1
CT bone density Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Autosomal recessiv spondyloepimetafyseal dysplasi Finding site False Bone structure Inferred relationship Some 1
Thanatophoric dysplasia, type 1 (disorder) Finding site True Bone structure Inferred relationship Some 1
Atelosteogenesis type 2 Finding site False Bone structure Inferred relationship Some 1
Neoplasm of bone Finding site True Bone structure Inferred relationship Some 1
Primary open reduction of fracture dislocation of joint with combined internal and external fixation (procedure) Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 3
Periartikulær osteotomi i forbindelse med ledsygdom Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Multipel osteotomi, ikke klassificeret andetsteds Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Prosthetic replacement of bone (procedure) Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Maintenance of electromagnetic bone stimulator Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Menkes kinky-hair syndrome Finding site False Bone structure Inferred relationship Some 1
Anden specificeret excision af knogle Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Ekstern fiksering af osteotomi, ikke klassificeret andetsteds Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
anden fraktur med luksation eller subluksation Finding site False Bone structure Inferred relationship Some 2
Bone immobilisation Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Filling of segmental defect by bone transport Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
anden specificeret protetisk erstatning af knogle Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
A rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasia. The disease has characteristics of progressive dwarfism with short trunk, protruding sternum, microcephaly and intellectual disability of varying severity. Caused by mutations of the DYM gene (18q21.1). The large majority of mutations identified in the gene predict a loss of function of its product. DYM is expressed in the majority of tissue and codes for Dymeclin, a protein that interacts with membranes of the Golgi apparatus, but its role within the cell is still unknown. Transmission is autosomal recessive. Finding site False Bone structure Inferred relationship Some 1
Multiple congenital exostosis Finding site False Bone structure Inferred relationship Some 1
Brachyolmia - Maroteaux type (disorder) Finding site True Bone structure Inferred relationship Some 1
Fucosidosis is an extremely rare lysosomal storage disorder with characteristics of a highly variable phenotype with common manifestations including neurologic deterioration, coarse facial features, growth retardation, and recurrent sinopulmonary infections, as well as seizures, visceromegaly, angiokeratoma and dysostosis. Finding site False Bone structure Inferred relationship Some 1
Diagnostisk punktur af knogle, ikke nærmere specificeret Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Anden periartikulær osteotomi, ikke nærmere specificeret Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Metaphyseal chondrodysplasia, Sedaghatian type (disorder) Finding site True Bone structure Inferred relationship Some 1
protetisk erstatning af knogle, ikke nærmere specificeret Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Partial ostectomy Procedure site - Direct (attribute) False Bone structure Inferred relationship Some 1
Revision to arthroscopic reduction of fracture Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Bone nailing Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
A rare genetic syndrome with characteristics of limb shortening and abnormalities of the head, face and external genitalia. Two forms of the syndrome with different patterns of inheritance and variable frequency of clinical signs have been described: a milder autosomal dominant form and a more severe autosomal recessive form. The syndrome has a wide clinical spectrum. Transmission is autosomal dominant or recessive. Finding site False Bone structure Inferred relationship Some 1
Benign autosomal dominant osteopetrose Finding site False Bone structure Inferred relationship Some 1
Removal of bone fragments (procedure) Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1
Defects of the tubular (and flat) bones and/or axial skeleton Finding site False Bone structure Inferred relationship Some 1
Thanatophoric dysplasia, type 2 (disorder) Finding site True Bone structure Inferred relationship Some 1
Lukket knoglefraktur, uspecificeret Finding site False Bone structure Inferred relationship Some 1
Spondylodysplasia, San Diego type Finding site False Bone structure Inferred relationship Some 1
Open fracture involving thorax with lower back and pelvis and limbs (disorder) Finding site False Bone structure Inferred relationship Some 1
Radiofrequency ablation of osteoid osteoma using computed tomography guidance (procedure) Procedure site - Direct (attribute) True Bone structure Inferred relationship Some 1

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