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54006005: Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3793710015 Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3793711016 Hereditary persistence of fetal hemoglobin delta beta plus thalassemia en Synonym Active Case insensitive SNOMED CT core
3793712011 Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia en Synonym Active Case insensitive SNOMED CT core
3793714012 Hereditary persistence of foetal haemoglobin delta beta plus thalassaemia en Synonym Active Case insensitive SNOMED CT core
3793721012 HPFH (hereditary persistence of fetal hemoglobin) delta beta plus thalassemia en Synonym Active Case sensitive SNOMED CT core
3793726019 HPFH (hereditary persistence of fetal haemoglobin) delta beta plus thalassaemia en Synonym Active Case sensitive SNOMED CT core
3793727011 HPFH (hereditary persistence of foetal haemoglobin) delta 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 delta beta plus thalassaemia Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 2
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Has definitional manifestation Erythropenia false Inferred relationship Some
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Finding site Haematopoietic system structure false Inferred relationship Some
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Is a Delta beta zero thalassaemia true Inferred relationship Some
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Is a Hereditary persistence of fetal haemoglobin thalassaemia true Inferred relationship Some
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Finding site Body system structure false Inferred relationship Some
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Has interpretation Below reference range false Inferred relationship Some 1
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Interprets Measurement of total haemoglobin concentration false Inferred relationship Some 1
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Has interpretation Below reference range true Inferred relationship Some 2
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Interprets Red blood cell count false Inferred relationship Some 2
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Occurrence Congenital true Inferred relationship Some 3
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Finding site Erythrocyte true Inferred relationship Some 3
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Finding site Haematopoietic system structure false Inferred relationship Some
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia Finding site Erythrocyte 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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