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443138004: Granulomatosis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2835362016 Granulomatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2842499012 Granulomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1842291000195114 granulomatosi it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5339841000241111 granulomatose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


13 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Granulomatosis (disorder) Is a Inflammatory disorder true Inferred relationship Some
Granulomatosis (disorder) Associated morphology Granulomatosis true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Orofacial granulomatosis of gingivae Is a True Granulomatosis (disorder) Inferred relationship Some
Bronchocentric granulomatosis Is a True Granulomatosis (disorder) Inferred relationship Some
Granulomatosis with polyangiitis of nose Is a True Granulomatosis (disorder) Inferred relationship Some
Granulomatosis with polyangiitis of larynx Is a True Granulomatosis (disorder) Inferred relationship Some
Intraspinal granuloma Is a True Granulomatosis (disorder) Inferred relationship Some
Intracranial granuloma Is a True Granulomatosis (disorder) Inferred relationship Some
Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder) Is a False Granulomatosis (disorder) Inferred relationship Some
Granulomatosis with polyangiitis of gingiva Is a True Granulomatosis (disorder) Inferred relationship Some
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. Is a False Granulomatosis (disorder) Inferred relationship Some
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. Is a True Granulomatosis (disorder) Inferred relationship Some
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. Is a True Granulomatosis (disorder) Inferred relationship Some
Lymphomatoid granulomatosis Is a False Granulomatosis (disorder) Inferred relationship Some
Lymphomatoid granulomatosis of lung (disorder) Is a False Granulomatosis (disorder) Inferred relationship Some

This concept is not in any reference sets

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