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234618008: Complement regulatory factor defect (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
351534013 Complement regulatory factor defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622963010 Complement regulatory factor defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
351534013 Complement regulatory factor defect en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
351534013 Complement regulatory factor defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622963010 Complement regulatory factor defect (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
622963010 Complement regulatory factor defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5862701000241116 défaut d'un facteur de régulation du complément fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5862701000241116 défaut d'un facteur de régulation du complément fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

14 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complement regulatory factor defect Is a Complement deficiency disease true Inferred relationship Existential restriction modifier (core metadata concept)
Complement regulatory factor defect Finding site Structure of immune system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Complement regulatory factor defect Is a Disorder of immune structure true Inferred relationship Existential restriction modifier (core metadata concept)
Complement regulatory factor defect Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
Complement regulatory factor defect 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
Factor I deficiency Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Factor H deficiency (disorder) Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Complement 4 binding protein deficiency Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Decay accelerating factor deficiency Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Homologous restriction factor deficiency Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Complement 5a inhibitor deficiency Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Anaphylotoxin inactivator deficiency Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Familial C3B inhibitor deficiency syndrome Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Is a False Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Primary CD59 deficiency Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Recurrent Neisseria infection due to factor D deficiency (disorder) Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary C1 esterase inhibitor deficiency - deficient factor Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor Is a True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept)
Atypical haemolytic uraemic syndrome with complement gene abnormality Due to True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept) 12
Atypical hemolytic uremic syndrome with anti-factor H antibodies Due to True Complement regulatory factor defect Inferred relationship Existential restriction modifier (core metadata concept) 12

This concept is not in any reference sets

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