443138004: Granulomatosis (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Inflammatory disorder\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

4746751000005111 granulomatose da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

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 disease with characteristics of 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 with characteristics of 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 cytopenia, 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