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234593008: Classical complement pathway abnormality (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
351505019 Classical complement pathway abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622934012 Classical complement pathway abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5842831000241112 anomalie de la voie classique du complément fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429131001000119 Immundefekt durch klassischen Komponentenmangel des Komplementsystems de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Classical complement pathway abnormality Is a Complement deficiency disease true Inferred relationship Some
Classical complement pathway abnormality Finding site Structure of immune system (body structure) true Inferred relationship Some 1
Classical complement pathway abnormality Is a Disorder of immune structure (disorder) true Inferred relationship Some
Classical complement pathway abnormality Has definitional manifestation Immune system finding false Inferred relationship Some
Classical complement pathway abnormality Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Complement 1q deficiency Is a True Classical complement pathway abnormality Inferred relationship Some
Complement 1r deficiency Is a True Classical complement pathway abnormality Inferred relationship Some
Complement 1s deficiency Is a True Classical complement pathway abnormality Inferred relationship Some
Complement 2 deficiency Is a True Classical complement pathway abnormality Inferred relationship Some
Complement 4 deficiency Is a True Classical complement pathway abnormality Inferred relationship Some
Complement 4A deficiency Is a True Classical complement pathway abnormality Inferred relationship Some
Complement 4B deficiency Is a True Classical complement pathway abnormality Inferred relationship Some
Complement 3 deficiency Is a False Classical complement pathway abnormality Inferred relationship Some
Complement component 3 deficiency is a rare, genetic, primary immunodeficiency characterized by susceptibility to infection (mainly by gram negative bacteria) due to extremely low C3 plasma levels. Patients typically present recurrent episodes of sinusitis, tonsillitis, and/or otitis, as well as upper and lower respiratory tract infections (including pneumonia) and skin infections, such as erythema multiforme. Autoimmune disease resembling systemic lupus erythematosus and mesangiocapillary or membranoproliferative glomerulonephritis may develop, resulting in renal failure. Is a True Classical complement pathway abnormality Inferred relationship Some

This concept is not in any reference sets

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