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61395005: Hereditary persistence of fetal hemoglobin G gamma 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
102000014 HPFH G gamma beta^+^ thalassemia en Synonym Inactive Entire term case sensitive SNOMED CT core module
498999014 HPFH G gamma beta^+^ thalassaemia en Synonym Inactive Entire term case sensitive SNOMED CT core module
800452017 HPFH G gamma beta^+^ thalassemia (disorder) en Fully specified name Inactive Entire term case sensitive SNOMED CT core module
2612458011 Hereditary persistence of fetal hemoglobin (HPFH) G gamma beta^+^ thalassemia (disorder) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
2620925018 Hereditary persistence of fetal haemoglobin (HPFH) G gamma beta^+^ thalassaemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
2620926017 Hereditary persistence of fetal hemoglobin (HPFH) G gamma beta^+^ thalassemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
2793196016 Hereditary persistence of foetal haemoglobin (HPFH) G gamma beta^+^ thalassaemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
2914079019 Hereditary persistence of fetal hemoglobin G gamma beta^+^ thalassemia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
2915152013 Hereditary persistence of fetal hemoglobin G gamma beta^+^ thalassemia (disorder) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
3793694018 Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia en Synonym Active Only initial character case insensitive SNOMED CT core module
3793695017 Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia en Synonym Active Only initial character case insensitive SNOMED CT core module
3793698015 Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3800043011 HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia en Synonym Active Entire term case sensitive SNOMED CT core module
3800044017 HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia en Synonym Active Entire term case sensitive SNOMED CT core module
3800045016 HPFH (hereditary persistence of foetal haemoglobin) G gamma 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 G gamma beta plus thalassemia Is a Hereditary persistence of fetal hemoglobin thalassemia true Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Is a Beta plus thalassemia true Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Has interpretation Below reference range false Inferred relationship Existential restriction modifier 1
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Interprets Measurement of total hemoglobin concentration false Inferred relationship Existential restriction modifier 1
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Interprets Red blood cell count false Inferred relationship Existential restriction modifier 2
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Erythrocyte true Inferred relationship Existential restriction modifier 3
Hereditary persistence of fetal hemoglobin G gamma 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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