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32855007: Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (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
54830012 HPFH unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2620581019 Hereditary persistence of fetal hemoglobin (HPF) unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2793477014 Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2913546016 Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2914016017 Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3014153015 Hereditary persistence of fetal haemoglobin unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
54830012 HPFH unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
764188019 HPFH unlinked to beta-globulin gene cluster (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
764188019 HPFH unlinked to beta-globulin gene cluster (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2611884011 Hereditary persistence of fetal hemoglobin (HPF) unlinked to beta-globulin gene cluster (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2620581019 Hereditary persistence of fetal hemoglobin (HPF) unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2620582014 Hereditary persistence of fetal haemoglobin (HPF) unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2793477014 Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2913546016 Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2913546016 Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2914016017 Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2914016017 Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3014153015 Hereditary persistence of fetal haemoglobin unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3014153015 Hereditary persistence of fetal haemoglobin unlinked to beta-globulin gene cluster en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6299901000241116 PHHF (persistance héréditaire d'hémoglobine fœtale) non liée au groupe de gènes des bêtaglobulines fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6299911000241119 persistance héréditaire d'hémoglobine fœtale non liée au groupe de gènes des bêtaglobulines fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6299901000241116 PHHF (persistance héréditaire d'hémoglobine fœtale) non liée au groupe de gènes des bêtaglobulines fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6299911000241119 persistance héréditaire d'hémoglobine fœtale non liée au groupe de gènes des bêtaglobulines fr Synonym (core metadata concept) Active Entire term case insensitive (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 foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Is a Hereditary persistence of fetal hemoglobin thalassemia true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Interprets Measurement of total haemoglobin concentration false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Interprets Red blood cell count false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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