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1055261006: Fibro-osseous pseudotumor (morphologic abnormality)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4283309010 Fibro-osseous pseudotumor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4283310017 Fibro-osseous pseudotumor (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4283311018 Fibro-osseous pseudotumour en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibro-osseous pseudotumor Is a Osseous metaplasia true Inferred relationship Some
Fibro-osseous pseudotumor Is a Reactive fibrosis (morphologic abnormality) true Inferred relationship Some
Fibro-osseous pseudotumor Is a Pseudotumor true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Fibro-osseous pseudotumor of skin of digit (disorder) Associated morphology True Fibro-osseous pseudotumor Inferred relationship Some 1
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. Associated morphology False Fibro-osseous pseudotumor Inferred relationship Some 1

This concept is not in any reference sets

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