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234619000: Hereditary C1 esterase inhibitor deficiency - deficient factor (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
2161482011 Hereditary angioedema - type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
351535014 Hereditary C1 esterase inhibitor deficiency - deficient factor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
351536010 C1 esterase inhibitor deficiency - type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
351537018 Hereditary angioneurotic oedema - type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
351538011 Hereditary angio-oedema - type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
351540018 Hereditary angioneurotic edema - type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622964016 Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary C1 esterase inhibitor deficiency - deficient factor Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Some 3
Hereditary C1 esterase inhibitor deficiency - deficient factor Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 2
Hereditary C1 esterase inhibitor deficiency - deficient factor est un(e) (attribut) Hereditary disorder of immune system true Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor est un(e) (attribut) Complement regulatory factor defect true Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor morphologie associée (attribut) Angioedema true Inferred relationship Some 1
Hereditary C1 esterase inhibitor deficiency - deficient factor est un(e) (attribut) Angioedema due to disorder of kinin metabolism true Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor Causative agent Kallidin I (substance) true Inferred relationship Some 1
Hereditary C1 esterase inhibitor deficiency - deficient factor est un(e) (attribut) Hereditary angioedema with C1Inh (C1 esterase inhibitor) deficiency true Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor morphologie associée (attribut) inflammation false Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor est défini par la manifestation de (attribut) Immune system finding false Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor est un(e) (attribut) Hereditary angioedema false Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor est un(e) (attribut) Angioedema due to disorder of C1 esterase inhibitor (disorder) false Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor localisation d'une constatation (attribut) structure du système immunitaire true Inferred relationship Some 2
Hereditary C1 esterase inhibitor deficiency - deficient factor localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some
Hereditary C1 esterase inhibitor deficiency - deficient factor morphologie associée (attribut) Urticaria false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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