66729008: Hemoglobin D disease (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\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin D disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
110848014	Hemoglobin D disease	en	Synonym	Active	Case sensitive	SNOMED CT core
110849018	Hemoglobin D-D disease	en	Synonym	Active	Case sensitive	SNOMED CT core
500508012	Homozygous for Hb D	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
500509016	Haemoglobin D disease	en	Synonym	Active	Case sensitive	SNOMED CT core
500510014	Haemoglobin D-D disease	en	Synonym	Active	Case sensitive	SNOMED CT core
806374019	Hemoglobin D disease (disorder)	en	Fully specified name	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

Back to Start