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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
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
5084160015 A rare genetic primary bone dysplasia with characteristics of 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
5084161016 A rare genetic primary bone dysplasia with characteristics of 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
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
3453731001000115 Osteofibröse Dysplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3453731001000115 Osteofibröse Dysplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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