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725049005: Aggressive fibromatosis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3437473018 Aggressive fibromatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3437474012 Aggressive fibromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3437475013 Desmoid type fibromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3437476014 Desmoid tumor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3437477017 Desmoid tumour en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3773008016 Desmoid fibromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3773009012 Deep fibromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3437478010 Desmoid tumor can occur in any part of the body: extra-abdominally (neck, shoulders, upper limbs, gluteal region), abdominally (originating from muscle fascia or the abdominal/chest wall), and more rarely intra-abdominally in the mesentery or retroperitoneum. Depending on the location of the tumor, symptoms may include pain, fever and functional impairment or loss of function of the organ involved. Desmoid tumor results from the proliferation of well-differentiated myofibroblasts. The exact etiopathogenetic mechanism is still unknown, but they seem to have a multi-factorial origin with hormonal and genetic factors being involved. Somatic mutations in the CTNNB1 gene (3q21) encoding beta-catenin have been found in about 85 % of sporadic cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3437479019 Desmoid tumour can occur in any part of the body: extra-abdominally (neck, shoulders, upper limbs, gluteal region), abdominally (originating from muscle fascia or the abdominal/chest wall), and more rarely intra-abdominally in the mesentery or retroperitoneum. Depending on the location of the tumour, symptoms may include pain, fever and functional impairment or loss of function of the organ involved. Desmoid tumour results from the proliferation of well-differentiated myofibroblasts. The exact aetiopathogenetic mechanism is still unknown, but they seem to have a multi-factorial origin with hormonal and genetic factors being involved. Somatic mutations in the CTNNB1 gene (3q21) encoding beta-catenin have been found in about 85% of sporadic cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
7750911000172116 fibromatose de type desmoïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
7750921000172114 tumeur desmoïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
7750931000172112 fibromatose agressive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4365421000172112 agressieve fibromatose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aggressive fibromatosis (disorder) Associated morphology Aggressive fibromatosis true Inferred relationship Some 1
Aggressive fibromatosis (disorder) Is a Neoplastic disease of uncertain behavior true Inferred relationship Some
Aggressive fibromatosis (disorder) Is a Fibromatosis (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Aggressive infantile fibromatosis Is a True Aggressive fibromatosis (disorder) Inferred relationship Some
Aggressive fibromatosis of breast (disorder) Is a True Aggressive fibromatosis (disorder) Inferred relationship Some
Extra-abdominal fibromatosis (disorder) Is a True Aggressive fibromatosis (disorder) Inferred relationship Some
Desmoid fibromatosis of skin Is a True Aggressive fibromatosis (disorder) Inferred relationship Some
Abdominal fibromatosis (disorder) Is a True Aggressive fibromatosis (disorder) Inferred relationship Some

Reference Sets

Belgian subset for medical problems in patient health records

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