782909004: Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\Haemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Haemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation

Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3756649011	Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3756650011	Haemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3756651010	Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3756652015	A rare genetic constitutional coagulation factor defect disorder characterized by a bleeding tendency of variable severity due to methionine 358 to arginine replacement (Pittsburgh mutation) in the alpha-1-antitrypsin protein. Patients present with spontaneous hematomas, hematomas following minor trauma or surgery and in female patients ovarian hematomas after ovulation.	en	Definition	Active	Case sensitive	SNOMED CT core
3756653013	A rare genetic constitutional coagulation factor defect disorder characterised by a bleeding tendency of variable severity due to methionine 358 to arginine replacement (Pittsburgh mutation) in the alpha-1-antitrypsin protein. Patients present with spontaneous haematomas, haematomas following minor trauma or surgery and in female patients ovarian haematomas after ovulation.	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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