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54006005: Hereditary persistence of fetal hemoglobin delta beta plus 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
89768011 HPFH delta beta^0^ thalassemia en Synonym Inactive Entire term case sensitive SNOMED CT core module
496831019 HPFH delta beta^0^ thalassaemia en Synonym Inactive Entire term case sensitive SNOMED CT core module
792190012 HPFH delta beta^0^ thalassemia (disorder) en Fully specified name Inactive Entire term case sensitive SNOMED CT core module
2612423014 Hereditary persistence of fetal hemoglobin (HPFH) delta beta^0^ thalassemia (disorder) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
2620864016 Hereditary persistence of fetal hemoglobin (HPFH) delta beta^0^ thalassemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
2620865015 Hereditary persistence of fetal haemoglobin (HPFH) delta beta^0^ thalassaemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
2793507013 Hereditary persistence of foetal haemoglobin (HPFH) delta beta^0^ thalassaemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
2914025011 Hereditary persistence of fetal hemoglobin delta beta^0^ thalassemia en Synonym Inactive Entire term case insensitive SNOMED CT core module
2915272012 Hereditary persistence of fetal hemoglobin delta beta^0^ thalassemia (disorder) en Fully specified name Inactive Entire term case insensitive SNOMED CT core module
3014106018 Hereditary persistence of fetal haemoglobin delta beta^0^ thalassaemia en Synonym Inactive Entire term case insensitive SNOMED CT core module
3793710015 Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3793711016 Hereditary persistence of fetal hemoglobin delta beta plus thalassemia en Synonym Active Entire term case insensitive SNOMED CT core module
3793712011 Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia en Synonym Active Entire term case insensitive SNOMED CT core module
3793714012 Hereditary persistence of foetal haemoglobin delta beta plus thalassaemia en Synonym Active Entire term case insensitive SNOMED CT core module
3793721012 HPFH (hereditary persistence of fetal hemoglobin) delta beta plus thalassemia en Synonym Active Entire term case sensitive SNOMED CT core module
3793726019 HPFH (hereditary persistence of fetal haemoglobin) delta beta plus thalassaemia en Synonym Active Entire term case sensitive SNOMED CT core module
3793727011 HPFH (hereditary persistence of foetal haemoglobin) delta beta plus thalassaemia en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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