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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. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3758297010 Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3758298017 Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3758299013 Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


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 Existential restriction modifier
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Is a Hereditary persistence of fetal hemoglobin true Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Is a Sickling disorder due to hemoglobin S true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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