774084003: Neonatal antiphospholipid syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Thrombophilia\Acquired thrombophilia\Antiphospholipid syndrome\Neonatal antiphospholipid syndrome
• \Finding of neonate\Neonatal disorder\Neonatal antiphospholipid syndrome
• \Disease\Disorder of immune function\Autoimmune disease\Antiphospholipid syndrome\Neonatal antiphospholipid syndrome
• \Disease\Disorder of fetus or newborn\Neonatal disorder\Neonatal antiphospholipid syndrome
• \Disease\Disorder of haemostatic system\Thrombophilia\Acquired thrombophilia\Antiphospholipid syndrome\Neonatal antiphospholipid syndrome

Status: current, Defined. 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	Case insensitive	SNOMED CT core
3727916013	Neonatal antiphospholipid syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3727917016	Neonatal Hughes syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3727918014	Neonatal antiphospholipid antibody syndrome	en	Synonym	Active	Case insensitive	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	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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