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765202001: Familial multiple benign meningioma (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3657440013 Familial multiple benign meningioma en Synonym Active Case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial multiple benign meningioma Associated morphology Benign meningioma true Inferred relationship Some 1
Familial multiple benign meningioma Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Familial multiple benign meningioma Is a Hereditary disorder of nervous system true Inferred relationship Some
Familial multiple benign meningioma Is a Benign meningioma true Inferred relationship Some
Familial multiple benign meningioma Associated morphology Benign meningioma false Inferred relationship Some 1
Familial multiple benign meningioma Is a Familial neoplastic disease true Inferred relationship Some
Familial multiple benign meningioma Finding site Meninges structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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