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1234828008: Osteofibrous dysplasia (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
5084157010 Osteofibrous dysplasia en Synonym Active Case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteofibrous dysplasia Is a Congenital skeletal dysplasia true Inferred relationship Some
Osteofibrous dysplasia Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Osteofibrous dysplasia Is a Disorder of lower leg true Inferred relationship Some
Osteofibrous dysplasia Is a Heterotopic ossification true Inferred relationship Some
Osteofibrous dysplasia Is a Degenerative disorder of bone true Inferred relationship Some
Osteofibrous dysplasia Is a Developmental hereditary disorder true Inferred relationship Some
Osteofibrous dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Osteofibrous dysplasia Is a Finding of bone of lower limb true Inferred relationship Some
Osteofibrous dysplasia Occurrence Congenital true Inferred relationship Some 2
Osteofibrous dysplasia Finding site Skeletal system structure true Inferred relationship Some 2
Osteofibrous dysplasia Associated morphology Dysplasia true Inferred relationship Some 2
Osteofibrous dysplasia Pathological process Pathological developmental process true Inferred relationship Some 2
Osteofibrous dysplasia Finding site Bone structure of lower leg true Inferred relationship Some 1
Osteofibrous dysplasia Associated morphology Fibro-osseous pseudotumour true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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