FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

16402000: Sickle cell trait (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1221346019 AS - Sickle cell trait en Synonym Active Case sensitive SNOMED CT core
1221347011 Heterozygous for Hb S en Synonym Active Initial character case insensitive SNOMED CT core
195756013 Drepanocytosis en Synonym Active Case insensitive SNOMED CT core
2164217010 RBC's - sickle cells present en Synonym Active Case sensitive SNOMED CT core
2164218017 Sickle cells present en Synonym Active Case insensitive SNOMED CT core
27766012 Sickle cell trait en Synonym Active Case insensitive SNOMED CT core
27767015 Hemoglobin S-A disorder en Synonym Active Case sensitive SNOMED CT core
27768013 Hemoglobin A-S genotype en Synonym Active Case sensitive SNOMED CT core
27769017 Hemoglobin S trait en Synonym Active Case sensitive SNOMED CT core
27770016 Heterozygous hemoglobin S en Synonym Active Initial character case insensitive SNOMED CT core
477774011 Haemoglobin A-S genotype en Synonym Active Case sensitive SNOMED CT core
477775012 Haemoglobin S-A disorder en Synonym Active Case sensitive SNOMED CT core
477776013 Haemoglobin S trait en Synonym Active Case sensitive SNOMED CT core
477777016 Heterozygous haemoglobin S en Synonym Active Initial character case insensitive SNOMED CT core
743422014 Sickle cell trait (disorder) en Fully specified name Active Case insensitive SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sickle cell trait Is a Haemoglobinopathy false Inferred relationship Some
Sickle cell trait Finding site Haematopoietic system structure false Inferred relationship Some
Sickle cell trait Has definitional manifestation Red blood cell finding false Inferred relationship Some
Sickle cell trait Is a Hereditary haemoglobin S true Inferred relationship Some
Sickle cell trait Is a Heterozygous haemoglobinopathy true Inferred relationship Some
Sickle cell trait Finding site Body system structure false Inferred relationship Some
Sickle cell trait Occurrence Congenital true Inferred relationship Some 1
Sickle cell trait Finding site Erythrocyte true Inferred relationship Some 1
Sickle cell trait Finding site Haematopoietic system structure false Inferred relationship Some
Sickle cell trait Finding site Erythrocyte false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Gouty arthropathy due to sickle-cell trait Due to True Sickle cell trait Inferred relationship Some 3
Glomerular disorder due to sickle cell trait Due to True Sickle cell trait Inferred relationship Some 2
Retinopathy due to sickle cell trait Due to True Sickle cell trait Inferred relationship Some 2
Sickle cell trait with coexistent alpha-thalassaemia Is a True Sickle cell trait Inferred relationship Some
Suspected sickle cell trait Associated finding False Sickle cell trait Inferred relationship Some 1
Sickle cell trait not suspected Associated finding False Sickle cell trait Inferred relationship Some 1
Sickle cell trait not suspected Associated finding True Sickle cell trait Inferred relationship Some 1
Suspected sickle cell trait Associated finding True Sickle cell trait Inferred relationship Some 1
FH: Sickle cell trait Associated finding True Sickle cell trait Inferred relationship Some 1
FH: Sickle cell trait Associated finding False Sickle cell trait Inferred relationship Some 1
Sickle cell trait in mother complicating childbirth Is a True Sickle cell trait Inferred relationship Some
Sickle cell trait in mother complicating pregnancy Is a True Sickle cell trait Inferred relationship Some
FH: Sickle cell anaemia Associated finding False Sickle cell trait Inferred relationship Some
FH: Sickle cell trait Associated finding False Sickle cell trait Inferred relationship Some 1

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start