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39674000: Familial C3B inhibitor deficiency syndrome (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
66901019 Familial C3B inhibitor deficiency syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
776173013 Familial C3B inhibitor deficiency syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core 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
Familial C3B inhibitor deficiency syndrome Is a Hereditary disorder of immune system true Inferred relationship Existential restriction modifier
Familial C3B inhibitor deficiency syndrome Is a Familial disease true Inferred relationship Existential restriction modifier
Familial C3B inhibitor deficiency syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Familial C3B inhibitor deficiency syndrome Finding site Structure of immune system true Inferred relationship Existential restriction modifier 1
Familial C3B inhibitor deficiency syndrome Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Familial C3B inhibitor deficiency syndrome 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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