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1234828008: Osteofibrous dysplasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5084156018 Osteofibrous dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5084157010 Osteofibrous dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400225012 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400226013 Osteofibrous dysplasia is a rare, genetic primary bone dysplasia characterised by the presence of a benign, fibro-osseous, osteolytic tumour 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteofibrous dysplasia (disorder) Is a Skeletal dysplasia true Inferred relationship Some
Osteofibrous dysplasia (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Osteofibrous dysplasia (disorder) Is a Disorder of lower leg (disorder) false Inferred relationship Some
Osteofibrous dysplasia (disorder) Is a Heterotopic ossification false Inferred relationship Some
Osteofibrous dysplasia (disorder) Is a Degenerative disorder of bone false Inferred relationship Some
Osteofibrous dysplasia (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Osteofibrous dysplasia (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Osteofibrous dysplasia (disorder) Is a Finding of bone of lower limb (finding) false Inferred relationship Some
Osteofibrous dysplasia (disorder) Occurrence Congenital true Inferred relationship Some 2
Osteofibrous dysplasia (disorder) Finding site Skeletal system structure true Inferred relationship Some 2
Osteofibrous dysplasia (disorder) Associated morphology Dysplasia true Inferred relationship Some 2
Osteofibrous dysplasia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Osteofibrous dysplasia (disorder) Finding site Bone structure of lower leg true Inferred relationship Some 1
Osteofibrous dysplasia (disorder) Associated morphology Fibro-osseous pseudotumor false Inferred relationship Some 1
Osteofibrous dysplasia (disorder) Is a Neoplasm of lower leg (disorder) true Inferred relationship Some
Osteofibrous dysplasia (disorder) Is a Benign osteogenic neoplasm of bone of limb (disorder) true Inferred relationship Some
Osteofibrous dysplasia (disorder) Is a Benign neoplasm of bone of lower limb true Inferred relationship Some
Osteofibrous dysplasia (disorder) Associated morphology Osteofibrous dysplasia (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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