FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

16402000: Sickle cell trait (disorder)


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


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sickle cell trait Is a Hemoglobinopathy false Inferred relationship Existential restriction modifier
Sickle cell trait Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Sickle cell trait Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Sickle cell trait Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Sickle cell trait Has definitional manifestation Red blood cell finding false Inferred relationship Existential restriction modifier
Sickle cell trait Is a Hereditary hemoglobin S true Inferred relationship Existential restriction modifier
Sickle cell trait Is a Heterozygous hemoglobinopathy true Inferred relationship Existential restriction modifier
Sickle cell trait Finding site Body system structure false Inferred relationship Existential restriction modifier
Sickle cell trait Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Sickle cell trait Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Sickle cell trait with coexistent alpha-thalassemia Is a True Sickle cell trait Inferred relationship Existential restriction modifier
Family history of sickle cell anemia Associated finding False Sickle cell trait Inferred relationship Existential restriction modifier
Family history: Sickle cell trait Associated finding False Sickle cell trait Inferred relationship Existential restriction modifier 1
Suspected sickle cell trait Associated finding False Sickle cell trait Inferred relationship Existential restriction modifier 1
Sickle cell trait not suspected Associated finding False Sickle cell trait Inferred relationship Existential restriction modifier 1
Sickle cell trait not suspected Associated finding True Sickle cell trait Inferred relationship Existential restriction modifier 1
Suspected sickle cell trait Associated finding True Sickle cell trait Inferred relationship Existential restriction modifier 1
Family history: Sickle cell trait Associated finding True Sickle cell trait Inferred relationship Existential restriction modifier 1
Family history: Sickle cell trait Associated finding False Sickle cell trait Inferred relationship Existential restriction modifier 1
Sickle cell trait in mother complicating childbirth Is a True Sickle cell trait Inferred relationship Existential restriction modifier
Sickle cell trait in mother complicating pregnancy Is a True Sickle cell trait Inferred relationship Existential restriction modifier
Gouty arthropathy due to sickle-cell trait Due to True Sickle cell trait Inferred relationship Existential restriction modifier 3
Disorder of glomerulus due to sickle cell trait Due to True Sickle cell trait Inferred relationship Existential restriction modifier 2
Disorder of retina due to sickle cell trait Due to True Sickle cell trait Inferred relationship Existential restriction modifier 2
Suspected sickle cell disease Associated finding False Sickle cell trait Inferred relationship Existential restriction modifier 1
National Health Service Sickle Cell and Thalassaemia Screening Programme result consistent with haemoglobin S carrier (situation) Associated finding True Sickle cell trait Inferred relationship Existential restriction modifier 1
Sickle cell trait not suspected, no other haemoglobin or thalassaemia excluded Associated finding True Sickle cell trait Inferred relationship Existential restriction modifier 1
Haemoglobin S not suspected (by deoxyribonucleic acid), no other haemoglobin or thalassaemia excluded (situation) Associated finding True Sickle cell trait Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

Back to Start