190810006: Benign primary hypergammaglobulinemic purpura (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Skin AND/OR mucosa finding\Skin finding\Bleeding skin\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura

\General finding of soft tissue\Skin finding\Bleeding skin\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\General finding of soft tissue\Skin finding\Disorder of skin\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\General finding of soft tissue\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura

\Bleeding\Purpura\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Bleeding\Bleeding skin\Purpuric disorder\Benign primary hypergammaglobulinemic purpura

\Functional finding\Disorder of hemostatic system\Purpuric disorder\Benign primary hypergammaglobulinemic purpura

\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Integumentary system finding\Skin finding\Bleeding skin\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Integumentary system finding\Skin finding\Disorder of skin\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura

\Disease\Purpura\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Disease\Disorder of hemostatic system\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Disease\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Purpuric disorder\Benign primary hypergammaglobulinemic purpura

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

Descriptions:

Id Description Lang Type Status Case? Module

293360011 Benign primary hypergammaglobulinemic purpura en Synonym Active Entire term case insensitive SNOMED CT core module

293361010 Benign primary hypergammaglobulinaemic purpura en Synonym Active Entire term case insensitive SNOMED CT core module

574438019 Benign primary hypergammaglobulinemic purpura (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Benign primary hypergammaglobulinemic purpura	Is a	Purpuric disorder	false	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Finding site	Blood vessel structure	false	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Associated morphology	Purpura	false	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Finding site	Peripheral vascular system structure	false	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Is a	Purpuric disorder	true	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Is a	Disorder of skin	false	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Associated morphology	Purpura	false	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Has definitional manifestation	Purpura	false	Inferred relationship	Existential restriction modifier
Benign primary hypergammaglobulinemic purpura	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	1
Benign primary hypergammaglobulinemic purpura	Associated morphology	Purpura	true	Inferred relationship	Existential restriction modifier	1
Benign primary hypergammaglobulinemic purpura	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier	2
Benign primary hypergammaglobulinemic purpura	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
293360011	Benign primary hypergammaglobulinemic purpura	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
293361010	Benign primary hypergammaglobulinaemic purpura	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
574438019	Benign primary hypergammaglobulinemic purpura (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module