725105006: Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Functional finding\Disorder of haemostatic system\...
• \Blood coagulation disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Disease\Blood disease\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Disease\Blood disease\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Disease\Disorder of haemostatic system\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Disease\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency

Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3438645010	Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3438646011	Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3438647019	Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3438648012	A rare hematologic disease due to defective platelet function and characterized by mucocutaneous bleeding starting in infancy (around 18 months of age), presenting with prolonged and severe epistaxis, hematoma and bleeding after tooth extraction. Massive menorrhagia and chronic anemia have also been reported.	en	Definition	Active	Case sensitive	SNOMED CT core
3438649016	A rare haematologic disease due to defective platelet function and characterised by mucocutaneous bleeding starting in infancy (around 18 months of age), presenting with prolonged and severe epistaxis, haematoma and bleeding after tooth extraction. Massive menorrhagia and chronic anaemia have also been reported.	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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