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783254003: Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3758297010 Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3758298017 Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3758299013 Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3758300017 A rare genetic hemoglobinopathy characterized by generally mild clinical phenotype, high fetal hemoglobin levels and mild microcytosis and hypochromia. In some cases, acute sickle cell disease manifestations were reported, namely acute chest syndrome and acute pain crisis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3758301018 A rare genetic haemoglobinopathy characterised by generally mild clinical phenotype, high fetal haemoglobin levels and mild microcytosis and hypochromia. In some cases, acute sickle cell disease manifestations were reported, namely acute chest syndrome and acute pain crisis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
12741801000172117 syndrome de persistance héréditaire d'hémoglobine fœtale avec drépanocytose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
12741811000172119 syndrome de PHHF (persistance héréditaire d'hémoglobine fœtale) avec drépanocytose fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4945991000172117 syndroom van hereditaire persistentie van foetaal hemoglobine met sikkelcelziekte nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4946001000172116 syndroom van hereditaire persistentie van HbF met sikkelcelziekte nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4946011000172118 syndroom van erfelijke persistentie van foetaal hemoglobine met sikkelcelziekte nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4946021000172111 syndroom van HPFH met sikkelcelziekte nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Occurrence Congenital true Inferred relationship Some 1
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Finding site Erythrocyte true Inferred relationship Some 1
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Is a Hereditary persistence of fetal hemoglobin true Inferred relationship Some
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Is a Sickling disorder due to hemoglobin S (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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