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1144805008: Microscopic polyangiitis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: IPS terminology module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module
4543360019 Microscopic polyarteritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
4543361015 MPA - microscopic polyangiitis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)
4543362010 Microscopic polyangiitis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
4543363017 Micropolyangiitis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
4543364011 Microscopic polyangiitis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
4543372013 A rare inflammatory necrotizing systemic vasculitis that affects predominantly small vessels (i.e. small arteries, arterioles, capillaries, venules) in multiple organs, including the kidney, the lungs, the skin and the peripheral nerves. This disease is an antineutrophil cytoplasmic autoantibodies (ANCA)-associated autoimmune disease with little or no immune complex deposition. Evidence indicates that ANCA can activate neutrophils and monocytes and cause them to attack vessel walls. en Definition Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)
4543373015 A rare inflammatory necrotising systemic vasculitis that affects predominantly small vessels (i.e. small arteries, arterioles, capillaries, venules) in multiple organs, including the kidney, the lungs, the skin and the peripheral nerves. This disease is an antineutrophil cytoplasmic autoantibodies (ANCA)-associated autoimmune disease with little or no immune complex deposition. Evidence indicates that ANCA can activate neutrophils and monocytes and cause them to attack vessel walls. en Definition Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microscopic polyangiitis (disorder) Is a Necrotizing vasculitis true Inferred relationship Some
Microscopic polyangiitis (disorder) Is a Procedure related finding true Inferred relationship Some
Microscopic polyangiitis (disorder) Is a Polyarteritis true Inferred relationship Some
Microscopic polyangiitis (disorder) Is a Primary systemic vasculitis (disorder) true Inferred relationship Some
Microscopic polyangiitis (disorder) Is a Autoimmune disease true Inferred relationship Some
Microscopic polyangiitis (disorder) Associated morphology Necrotizing inflammation true Inferred relationship Some 1
Microscopic polyangiitis (disorder) Finding site Structure of small blood vessel (organ) true Inferred relationship Some 1
Microscopic polyangiitis (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Some 1
Microscopic polyangiitis (disorder) Associated morphology Necrotizing inflammation true Inferred relationship Some 2
Microscopic polyangiitis (disorder) Finding site Systemic arterial structure true Inferred relationship Some 2
Microscopic polyangiitis (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Some 2
Microscopic polyangiitis (disorder) Has interpretation Detected true Inferred relationship Some 3
Microscopic polyangiitis (disorder) Interprets Antineutrophil cytoplasmic antibody measurement true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

International Patient Summary

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