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

• SNOMED CT Concept\constatation clinique\...
• \Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...
• \troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \anémie\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Disease\anomalie des éléments figurés du sang (trouble)\anémie\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type
• \Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\thalassémie\Hereditary persistence of fetal hemoglobin thalassemia\HPFH deletion type

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

Descriptions:

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

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

GB English

US English

Back to Start