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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
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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteofibrous dysplasia (disorder) est un(e) (attribut) Skeletal dysplasia true Inferred relationship Some
Osteofibrous dysplasia (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Osteofibrous dysplasia (disorder) est un(e) (attribut) Disorder of lower leg (disorder) true Inferred relationship Some
Osteofibrous dysplasia (disorder) est un(e) (attribut) Heterotopic ossification true Inferred relationship Some
Osteofibrous dysplasia (disorder) est un(e) (attribut) Degenerative disorder of bone true Inferred relationship Some
Osteofibrous dysplasia (disorder) est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Osteofibrous dysplasia (disorder) est un(e) (attribut) Hereditary disorder of musculoskeletal system true Inferred relationship Some
Osteofibrous dysplasia (disorder) est un(e) (attribut) Finding of bone of lower limb (finding) true Inferred relationship Some
Osteofibrous dysplasia (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Osteofibrous dysplasia (disorder) localisation d'une constatation (attribut) Skeletal system structure true Inferred relationship Some 2
Osteofibrous dysplasia (disorder) morphologie associée (attribut) dysplasie true Inferred relationship Some 2
Osteofibrous dysplasia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Osteofibrous dysplasia (disorder) localisation d'une constatation (attribut) Bone structure of lower leg true Inferred relationship Some 1
Osteofibrous dysplasia (disorder) morphologie associée (attribut) Fibro-osseous pseudotumor true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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