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765202001: Familial multiple benign meningioma (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3657439011 Familial multiple benign meningioma (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3657440013 Familial multiple benign meningioma en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial multiple benign meningioma Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial multiple benign meningioma Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Familial multiple benign meningioma Is a Benign meningioma true Inferred relationship Existential restriction modifier
Familial multiple benign meningioma Associated morphology Meningioma, benign, no International Classification of Diseases for Oncology subtype false Inferred relationship Existential restriction modifier 1
Familial multiple benign meningioma Is a Familial neoplastic disease true Inferred relationship Existential restriction modifier
Familial multiple benign meningioma Finding site Meninges structure true Inferred relationship Existential restriction modifier 1
Familial multiple benign meningioma Associated morphology Benign meningioma true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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