123772008: Homozygous hemoglobinopathy (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\Homozygous hemoglobinopathy
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
192261019	Homozygous hemoglobinopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
203427013	Homozygous haemoglobinopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
726889010	Homozygous hemoglobinopathy (disorder)	en	Fully specified name	Active	Case insensitive	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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