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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 (core metadata concept). 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 (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3793695017 Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3793698015 Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3800043011 HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3800044017 HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3800045016 HPFH (hereditary persistence of foetal haemoglobin) G gamma beta plus thalassaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


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 Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Is a Beta plus thalassemia true Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Erythrocyte false Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Hematopoietic system structure false Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Has definitional manifestation Erythropenia false Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Hematopoietic system structure false Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Body system structure false Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Has interpretation Below reference range false Inferred relationship Some 1
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Interprets Measurement of total haemoglobin concentration false Inferred relationship Some 1
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Has interpretation Below reference range true Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Interprets Red blood cell count false Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Occurrence Congenital true Inferred relationship Some 3
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Finding site Erythrocyte true Inferred relationship Some 3
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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