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44328006: Granulomatosis (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
73944013 Granulomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
781444013 Granulomatosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Granulomatosis Is a Granulomatous inflammation false Inferred relationship Some
Granulomatosis Is a Granulomatous inflammatory morphology (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Orofacial granulomatosis of gingivae Associated morphology False Granulomatosis Inferred relationship Some 1
North American cutaneous blastomycosis Associated morphology False Granulomatosis Inferred relationship Some 2
Granulomatosis with polyangiitis of nose Associated morphology True Granulomatosis Inferred relationship Some 1
Granulomatosis with polyangiitis of larynx Associated morphology True Granulomatosis Inferred relationship Some 1
Bronchocentric granulomatosis Associated morphology False Granulomatosis Inferred relationship Some 1
Orofacial granulomatosis of gingivae Associated morphology True Granulomatosis Inferred relationship Some 1
Bronchocentric granulomatosis Associated morphology True Granulomatosis Inferred relationship Some 1
Granulomatosis (disorder) Associated morphology True Granulomatosis Inferred relationship Some 1
Intraspinal granuloma Associated morphology False Granulomatosis Inferred relationship Some 2
Intraspinal subdural granuloma Associated morphology True Granulomatosis Inferred relationship Some 1
Intraspinal epidural granuloma Associated morphology True Granulomatosis Inferred relationship Some 1
Intracranial granuloma Associated morphology True Granulomatosis Inferred relationship Some 2
Intracranial epidural granuloma Associated morphology True Granulomatosis Inferred relationship Some 1
Intracranial subdural granuloma Associated morphology True Granulomatosis Inferred relationship Some 1
Intraspinal epidural granuloma Associated morphology True Granulomatosis Inferred relationship Some 2
Intraspinal granuloma Associated morphology True Granulomatosis Inferred relationship Some 1
Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder) Associated morphology False Granulomatosis Inferred relationship Some
Granulomatosis with polyangiitis of gingiva Associated morphology True Granulomatosis Inferred relationship Some 1
Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder) Associated morphology False Granulomatosis Inferred relationship Some 2
A rare systemic inflammatory disease with characteristics of early onset granulomatous arthritis, uveitis and skin rash. There are familial and sporadic forms of the same disease. The disease is due to an inherited or de novo mutation in the NOD2 gene (16q12), responsible for alterations in the innate immune response, inflammation and cell death. Associated morphology False Granulomatosis Inferred relationship Some 4
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. Associated morphology True Granulomatosis Inferred relationship Some 1
Lymphomatoid granulomatosis Associated morphology False Granulomatosis Inferred relationship Some 3
Lymphomatoid granulomatosis of lung (disorder) Associated morphology False Granulomatosis Inferred relationship Some 3
A rare, genetic, non-severe combined immunodeficiency disease characterised by immunodeficiency (manifested by recurrent and/or severe bacterial and viral infections), destructive noninfectious granulomas involving skin, mucosa and internal organs, and various autoimmune manifestations (including cytopenias, vitiligo, psoriasis, myasthenia gravis, enteropathy). Immunophenotypically, T-cell and B-cell lymphopenia, hypogammaglobulinaemia, abnormal specific antibody production and impaired T-cell function are observed. Associated morphology True Granulomatosis Inferred relationship Some 1

This concept is not in any reference sets

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