81166004: Properdin deficiency disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\Disorder of complement\Complement deficiency disease\Alternative pathway deficiency\Properdin deficiency disease

\Disorder of body system\Disorder of immune structure (disorder)\Alternative pathway deficiency\Properdin deficiency disease

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

134675016 Properdin deficiency disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

504630014 Properdin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

822407019 Properdin deficiency disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Properdin deficiency disease	Is a	Alternative pathway deficiency	true	Inferred relationship	Some
Properdin deficiency disease	Finding site	Structure of immune system (body structure)	true	Inferred relationship	Some	1
Properdin deficiency disease	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
Properdin deficiency disease	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	2

Inbound Relationships

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This concept is not in any reference sets