FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

774084003: syndrome des antiphospholipides néonatal (trouble)


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

Descriptions:

Id Description Lang Type Status Case? Module
3727915012 Neonatal antiphospholipid syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727916013 Neonatal antiphospholipid syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727917016 Neonatal Hughes syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3727918014 Neonatal antiphospholipid antibody syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
772241000241117 syndrome des antiphospholipides néonatal (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
952871000172111 APS (antiphospholipides) néonatal fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
965001000172112 syndrome des antiphospholipides néonatal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3727919018 A rare secondary neonatal autoimmune disease with characteristics of single or recurrent episodes of venous, arterial or mixed thrombosis in a neonate whose mother does not have antiphospholipid syndrome manifestations. Patients present positive antiphospholipid antibodies and may have additional abnormalities associated (for example cardiac valve disease, livedo reticularis, thrombocytopenia, nephropathy, neurological manifestations). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal antiphospholipid syndrome (disorder) est un(e) (attribut) syndrome des antiphospholipides true Inferred relationship Some
Neonatal antiphospholipid syndrome (disorder) est un(e) (attribut) Acquired thrombophilia (disorder) false Inferred relationship Some
Neonatal antiphospholipid syndrome (disorder) survenue (attribut) néonatal true Inferred relationship Some 1
Neonatal antiphospholipid syndrome (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Some 1
Neonatal antiphospholipid syndrome (disorder) est un(e) (attribut) Neonatal disorder true Inferred relationship Some
Neonatal antiphospholipid syndrome (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 2
Neonatal antiphospholipid syndrome (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 2
Neonatal antiphospholipid syndrome (disorder) Causative agent Anti-phospholipid autoantibody (substance) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start