85557000: Hereditary persistence of fetal hemoglobin deletion type (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Measurement finding\Finding of substance level\Finding of protein level\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Evaluation finding\Hematopoietic system finding\Hematology test outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\...
• \Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type
• \Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of fetal hemoglobin deletion type

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
141806018	HPFH deletion type	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
141807010	HPFH deletion type, NOS	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
827635016	HPFH deletion type (disorder)	en	Fully specified name	Inactive	Entire term case sensitive	SNOMED CT core module
2612758012	Hereditary persistence of fetal hemoglobin (HPFH) deletion type (disorder)	en	Fully specified name	Inactive	Only initial character case insensitive	SNOMED CT core module
2621336012	Hereditary persistence of fetal hemoglobin (HPFH) deletion type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2621337015	Hereditary persistence of fetal haemoglobin (HPFH) deletion type	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
2795252012	Hereditary persistence of foetal haemoglobin (HPFH) deletion type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2913396019	Hereditary persistence of fetal hemoglobin deletion type	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2913799012	Hereditary persistence of fetal hemoglobin deletion type (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3013769014	Hereditary persistence of fetal haemoglobin deletion type	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start