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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
6230271000241117 persistance héréditaire d'hémoglobine fœtale avec thalassémie G gamma bêta plus fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6230281000241115 PHHF (persistance héréditaire d'hémoglobine fœtale) avec thalassémie G gamma bêta plus fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 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 (cell) 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 érythropénie 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 (cell) 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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