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39674000: Familial C3B inhibitor deficiency syndrome (disorder)

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
66901019 Familial C3B inhibitor deficiency syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
776173013 Familial C3B inhibitor deficiency syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
66901019 Familial C3B inhibitor deficiency syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
776173013 Familial C3B inhibitor deficiency syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
125871000077112 syndrome familial de déficit en inhibiteurs du C3B fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
125871000077112 syndrome familial de déficit en inhibiteurs du C3B fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial C3B inhibitor deficiency syndrome Is a Complement regulatory factor defect true Inferred relationship Existential restriction modifier (core metadata concept)
Familial C3B inhibitor deficiency syndrome Is a Hereditary disorder of immune system true Inferred relationship Existential restriction modifier (core metadata concept)
Familial C3B inhibitor deficiency syndrome Is a Familial disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial C3B inhibitor deficiency syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Familial C3B inhibitor deficiency syndrome Finding site Structure of immune system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial C3B inhibitor deficiency syndrome Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
Familial C3B inhibitor deficiency syndrome Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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