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81166004: Properdin deficiency disease (disorder)


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
134675016 Properdin deficiency disease en Synonym Active Entire term case insensitive SNOMED CT core module
504630014 Properdin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
822407019 Properdin deficiency disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Properdin deficiency disease Is a Alternative pathway deficiency true Inferred relationship Existential restriction modifier
Properdin deficiency disease Finding site Structure of immune system true Inferred relationship Existential restriction modifier 1
Properdin deficiency disease Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Properdin deficiency disease Pathological process Abnormal immune process 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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