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765202001: Familial multiple benign meningioma (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3657439011 Familial multiple benign meningioma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3657440013 Familial multiple benign meningioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3657437013 A rare benign neoplasm of the central nervous system characterized by the development of multiple or rarely solitary meningioma in two or more blood relatives without other apparent syndromic manifestations. Depending on the localization, growth rate and size of the tumors, patients can present with subtle, gradually worsening or abrupt and severe neurological compromise or can be completely asymptomatic. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657438015 A rare benign neoplasm of the central nervous system characterised by the development of multiple or rarely solitary meningioma in two or more blood relatives without other apparent syndromic manifestations. Depending on the localisation, growth rate and size of the tumours, patients can present with subtle, gradually worsening or abrupt and severe neurological compromise or can be completely asymptomatic. 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
Familial multiple benign meningioma (disorder) morphologie associée (attribut) Benign meningioma true Inferred relationship Some 1
Familial multiple benign meningioma (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Familial multiple benign meningioma (disorder) est un(e) (attribut) Hereditary disorder of nervous system true Inferred relationship Some
Familial multiple benign meningioma (disorder) est un(e) (attribut) Benign meningioma (disorder) true Inferred relationship Some
Familial multiple benign meningioma (disorder) morphologie associée (attribut) Meningioma, benign, no International Classification of Diseases for Oncology subtype (morphologic abnormality) false Inferred relationship Some 1
Familial multiple benign meningioma (disorder) est un(e) (attribut) néoplasie familiale true Inferred relationship Some
Familial multiple benign meningioma (disorder) localisation d'une constatation (attribut) structure des méninges 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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