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774084003: Neonatal antiphospholipid syndrome (disorder)

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
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
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
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
3417171001000119 Anti-Phospholipid-Syndrom, neonatales de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
952871000172111 APS (antiphospholipides) néonatal fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
965001000172112 syndrome des antiphospholipides néonatal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
952871000172111 APS (antiphospholipides) néonatal fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
965001000172112 syndrome des antiphospholipides néonatal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3417171001000119 Anti-Phospholipid-Syndrom, neonatales de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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