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128491006: Heterotopic ossification (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2011. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
206840016 Heterotopic ossification en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2880569013 Heterotopic ossification (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
73641000077111 ossification hétérotopique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


71 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Heterotopic ossification Is a Abnormal bone formation false Inferred relationship Some
Heterotopic ossification Associated morphology Osseous metaplasia true Inferred relationship Some 1
Heterotopic ossification Finding site Bone structure false Inferred relationship Some
Heterotopic ossification Interprets Bone function false Inferred relationship Some
Heterotopic ossification Is a General finding of soft tissue false Inferred relationship Some
Heterotopic ossification Finding site Structure of soft tissue (body structure) false Inferred relationship Some
Heterotopic ossification Finding site Bone structure false Inferred relationship Some
Heterotopic ossification Is a Bipartite ossification false Inferred relationship Some
Heterotopic ossification Has interpretation Abnormal false Inferred relationship Some 1
Heterotopic ossification Interprets Bone formation false Inferred relationship Some 1
Heterotopic ossification Is a calcification extrasquelettique false Inferred relationship Some
Heterotopic ossification Is a Structure with calcium deposition. true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Ossifying fasciitis Is a True Heterotopic ossification Inferred relationship Some
Ossifying pachymeningitis Is a True Heterotopic ossification Inferred relationship Some
Postoperative heterotopic ossification (disorder) Is a True Heterotopic ossification Inferred relationship Some
Heterotopic ossification of joint (disorder) Is a True Heterotopic ossification Inferred relationship Some
Muscular ossification Is a True Heterotopic ossification Inferred relationship Some
Heterotopic ossification of tendon (disorder) Is a True Heterotopic ossification Inferred relationship Some
Ectopic bone tissue, congenital Is a True Heterotopic ossification Inferred relationship Some
Heterotopic ossification due to neurological disorder Is a True Heterotopic ossification Inferred relationship Some
Ossification of trachea (disorder) Is a True Heterotopic ossification Inferred relationship Some
Disseminated idiopathic skeletal hyperostosis Is a True Heterotopic ossification Inferred relationship Some
Pulmonary ossification Is a True Heterotopic ossification Inferred relationship Some
Fibro-osseous pseudotumor of skin of digit (disorder) Is a True Heterotopic ossification Inferred relationship Some
Osteoma cutis (disorder) Is a True Heterotopic ossification Inferred relationship Some
Ossification of subperiosteum due to and following traumatic injury (disorder) Is a True Heterotopic ossification Inferred relationship Some
Osteofibrous dysplasia is a rare, genetic primary bone dysplasia characterized by the presence of a benign, fibro-osseous, osteolytic tumor typically located in the tibia (occasionally the fibula, or both) and usually involving the anterior diaphyseal cortex with adjacent cortical expansion. It may on occasion be asymptomatic or may present with a palpable mass, pain, tenderness and/or anterior bowing of the tibia. Is a False Heterotopic ossification Inferred relationship Some

This concept is not in any reference sets

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