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1260127003: Granulomatous vasculitis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Dec 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5159267017 Granulomatous vasculitis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5159268010 Granulomatous vasculitis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


18 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Granulomatous vasculitis (disorder) Is a Granulomatous disorder true Inferred relationship Some
Granulomatous vasculitis (disorder) Is a Vasculitis (disorder) true Inferred relationship Some
Granulomatous vasculitis (disorder) Finding site Blood vessel structure (body structure) true Inferred relationship Some 1
Granulomatous vasculitis (disorder) Associated morphology Granulomatous inflammation true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
angéite granulomateuse du système nerveux central Is a False Granulomatous vasculitis (disorder) Inferred relationship Some
Allergic granulomatosis angiitis (disorder) Is a False Granulomatous vasculitis (disorder) Inferred relationship Some
A rare vasculitis characterized by mostly unilateral inflammation of the temporal artery affecting patients up to fifty years of age. Patients typically present with a lump in the temporal region or a prominent temporal artery and often have headaches. Males are more frequently affected than females, and major systemic symptoms, ocular complications, and a biological inflammatory syndrome are usually absent, although peripheral blood eosinophilia may be seen. Histopathological analysis shows arteritis predominantly of the intima with possible extension to the perivascular tissue. The presence of granuloma, giant cells or fibrinoid necrosis is rare. Clinical relapses after one episode are uncommon. Is a True Granulomatous vasculitis (disorder) Inferred relationship Some
Tuberculous cerebral arteritis Is a True Granulomatous vasculitis (disorder) Inferred relationship Some
Giant cell arteritis (disorder) Is a True Granulomatous vasculitis (disorder) Inferred relationship Some
Granulomatosis with polyangiitis Is a True Granulomatous vasculitis (disorder) Inferred relationship Some

This concept is not in any reference sets

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