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91689009: Body system structure (body structure)

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
151907017 Organ system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
509587013 Body system structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
835054011 Body system structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
151907017 Organ system en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
151907017 Organ system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
509587013 Body system structure en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
509587013 Body system structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
835054011 Body system structure (body structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
835054011 Body system structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
12681000077117 structure d'un système corporel fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
12681000077117 structure d'un système corporel fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

32409 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Body system structure Is a Anatomical structure true Inferred relationship Existential restriction modifier (core metadata concept)
Body system structure partie de Entire body as a whole (body structure) false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
A rare isolated constitutional thrombocytopenia characterized by abnormally large platelets. Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital autosomal recessive small-platelet thrombocytopenia (disorder) Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to interleukin 7 receptor deficiency (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to CD45 deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe combined immunodeficiency due to CORO1A deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 1
O'Brien active compression test Procedure site - Direct (attribute) True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Load and shift test Procedure site - Direct (attribute) True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Yocum shoulder impingement test (procedure) Procedure site - Direct (attribute) True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyper extension internal rotation test (procedure) Procedure site - Direct (attribute) True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Posterolateral rotatory drawer test of elbow (procedure) Procedure site - Direct (attribute) True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Tabletop relocation test (procedure) Procedure site - Direct (attribute) True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Pseudo von Willebrand disease Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
A group of rare monogenic primary immunodeficiency disorders characterized by a lack of functional peripheral T lymphocytes with presence of B lymphocytes, resulting in early-onset severe respiratory viral, bacterial, or fungal infections, diarrhea and failure to thrive. Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Severe combined immunodeficiency due to CORO1A deficiency Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Severe combined immunodeficiency due to LAT deficiency Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to CD45 deficiency Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to interleukin 7 receptor deficiency (disorder) Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to CD3 delta subunit of T-cell receptor complex mutation (disorder) Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to CD3 epsilon subunit of T-cell receptor complex mutation (disorder) Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive T- B+ severe combined immunodeficiency due to CD3Z mutation Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to SLP76 mutation (disorder) Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Severe combined immunodeficiency due to BCL11 transcription factor B deficiency (disorder) Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive combined immunodeficiency due to Wiskott Aldrich syndrome protein-interacting protein deficiency (disorder) Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect (disorder) Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 4

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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