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61395005: Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3793694018 Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia en Synonym Active Initial character case insensitive SNOMED CT core
3793695017 Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia en Synonym Active Initial character case insensitive SNOMED CT core
3793698015 Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3800043011 HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia en Synonym Active Case sensitive SNOMED CT core
3800044017 HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia en Synonym Active Case sensitive SNOMED CT core
3800045016 HPFH (hereditary persistence of foetal haemoglobin) G gamma beta plus thalassaemia en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 2
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Has definitional manifestation Erythropenia false Inferred relationship Some
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Finding site Haematopoietic system structure false Inferred relationship Some
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Is a Hereditary persistence of fetal haemoglobin thalassaemia true Inferred relationship Some
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Is a Beta plus thalassaemia true Inferred relationship Some
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Finding site Body system structure false Inferred relationship Some
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Has interpretation Below reference range false Inferred relationship Some 1
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Interprets Measurement of total haemoglobin concentration false Inferred relationship Some 1
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Has interpretation Below reference range true Inferred relationship Some 2
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Interprets Red blood cell count false Inferred relationship Some 2
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Occurrence Congenital true Inferred relationship Some 3
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Finding site Erythrocyte true Inferred relationship Some 3
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Finding site Erythrocyte false Inferred relationship Some
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia Finding site Haematopoietic system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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