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65959000: Beta thalassemia (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
500265014 Beta thalassemia en Synonym Active Entire term case insensitive SNOMED CT core module
500266010 Beta thalassemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
500267018 Beta thalassaemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
500268011 Beta thalassaemia en Synonym Active Entire term case insensitive SNOMED CT core module
3793602013 Beta thalassemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3800341019 beta thalassemia en Synonym Active Entire term case sensitive SNOMED CT core module
3800342014 beta thalassaemia en Synonym Active Entire term case sensitive SNOMED CT core module


30 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Beta thalassemia Is a Thalassemia true Inferred relationship Existential restriction modifier
Beta thalassemia Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Beta thalassemia Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Beta thalassemia Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
Beta thalassemia Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Beta thalassemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Beta thalassemia Has interpretation Below reference range false Inferred relationship Existential restriction modifier 1
Beta thalassemia Interprets Measurement of total hemoglobin concentration false Inferred relationship Existential restriction modifier 1
Beta thalassemia Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Beta thalassemia Interprets Red blood cell count false Inferred relationship Existential restriction modifier 2
Beta thalassemia Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Beta thalassemia Finding site Erythrocyte true Inferred relationship Existential restriction modifier 3
Beta thalassemia Interprets Measurement of total hemoglobin concentration true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Beta thalassemia intermedia Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Hemoglobin Lepore trait Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Delta-beta-Lepore thalassemia Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Beta thalassemia trait Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Delta beta thalassemia Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Homozygous beta thalassemia Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Beta plus thalassemia Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Beta zero thalassemia Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Sickle cell-beta-thalassemia Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Family history of beta thalassemia Associated finding True Beta thalassemia Inferred relationship Existential restriction modifier 1
Dominant beta-thalassemia Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Beta thalassemia X-linked thrombocytopenia syndrome Is a True Beta thalassemia Inferred relationship Existential restriction modifier
Hemoglobin E/beta thalassemia disease Is a True Beta thalassemia Inferred relationship Existential restriction modifier
National Health Service Sickle Cell and Thalassaemia Screening Programme result consistent with haemoglobin variant and/or beta-thalassaemia (situation) Associated finding True Beta thalassemia Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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