16402000: Sickle cell trait (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Finding of blood, lymphatics and immune system\Disorder of cellular component of blood (disorder)\...
• \Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\...
• \Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Heterozygous hemoglobinopathy\Sickle cell trait
• \Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait
• \Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait
• \Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait
• \Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait
• \Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait
• \Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait
• \Disease\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait
• \Disease\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait

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
27766012	Sickle cell trait	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
27767015	Hemoglobin S-A disorder	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
27768013	Hemoglobin A-S genotype	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
27769017	Hemoglobin S trait	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
27770016	Heterozygous hemoglobin S	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
195756013	Drepanocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
477774011	Haemoglobin A-S genotype	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
477775012	Haemoglobin S-A disorder	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
477776013	Haemoglobin S trait	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
477777016	Heterozygous haemoglobin S	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
743422014	Sickle cell trait (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1221346019	AS - Sickle cell trait	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1221347011	Heterozygous for Hb S	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2164217010	RBC's - sickle cells present	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2164218017	Sickle cells present	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
90811000172117	trait drépanocytaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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