782880001: Hemoglobinopathy Toms River (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Haemoglobinopathy Toms River
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Haemoglobinopathy Toms River

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3756529010	Haemoglobinopathy Toms River	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3756530017	Hemoglobinopathy Toms River (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3756531018	Hemoglobinopathy Toms River	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3756532013	Transient neonatal cyanosis and anemia due to Toms River Hemoglobin	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3756533015	Transient neonatal cyanosis and anaemia due to Toms River Haemoglobin	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3756534014	A rare genetic haemoglobinopathy disorder due to a defect in the gama subunit of the fetal haemoglobin and characterised by neonatal cyanosis, low haemoglobin oxygen saturation levels without arterial hypoxaemia, moderate anaemia and reticulocytosis, not associated with heart or lung disease. Symptoms progressively subside within the first months of life. Can be caused by heterozygous mutation in the HBG2 gene on chromosome 11p15.5.	en	Definition	Active	Case sensitive	SNOMED CT core
3756535010	A rare genetic hemoglobinopathy disorder due to a defect in the gama subunit of the fetal hemoglobin and characterized by neonatal cyanosis, low hemoglobin oxygen saturation levels without arterial hypoxemia, moderate anemia and reticulocytosis, not associated with heart or lung disease. Symptoms progressively subside within the first months of life. Can be caused by heterozygous mutation in the HBG2 gene on chromosome 11p15.5.	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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