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774084003: Neonatal antiphospholipid syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3727915012 Neonatal antiphospholipid syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3727916013 Neonatal antiphospholipid syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3727917016 Neonatal Hughes syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3727918014 Neonatal antiphospholipid antibody syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal antiphospholipid syndrome Is a Antiphospholipid syndrome true Inferred relationship Existential restriction modifier
Neonatal antiphospholipid syndrome Is a Acquired thrombophilia false Inferred relationship Existential restriction modifier
Neonatal antiphospholipid syndrome Occurrence Neonatal true Inferred relationship Existential restriction modifier 1
Neonatal antiphospholipid syndrome Pathological process Autoimmune process true Inferred relationship Existential restriction modifier 1
Neonatal antiphospholipid syndrome Is a Neonatal disorder true Inferred relationship Existential restriction modifier
Neonatal antiphospholipid syndrome Interprets Hemostatic function true Inferred relationship Existential restriction modifier 2
Neonatal antiphospholipid syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Neonatal antiphospholipid syndrome Causative agent Anti-phospholipid autoantibody true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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