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191201002: Hereditary persistence of fetal hemoglobin (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
294068017 Hb F disease en Synonym Active Entire term case sensitive SNOMED CT core module
294069013 HPFH - Hereditary persistence of fetal hemoglobin en Synonym Active Entire term case sensitive SNOMED CT core module
294070014 Hereditary persistence of fetal hemoglobin en Synonym Active Entire term case insensitive SNOMED CT core module
294071013 HPFH - Hereditary persistence of fetal haemoglobin en Synonym Active Entire term case sensitive SNOMED CT core module
294072018 Hereditary persistence of fetal haemoglobin en Synonym Active Entire term case insensitive SNOMED CT core module
574873011 Hereditary persistence of fetal hemoglobin (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2793120016 Hereditary persistence of foetal haemoglobin en Synonym Active Entire term case insensitive SNOMED CT core module
2793720014 HPFH - Hereditary persistence of foetal haemoglobin en Synonym Active Entire term case sensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary persistence of fetal hemoglobin Is a Hemoglobinopathy false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin Is a Hereditary red blood cell disorder false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin Has definitional manifestation Red blood cell finding false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin Is a Hereditary hemoglobinopathy true Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hereditary persistence of fetal hemoglobin Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Is a True Hereditary persistence of fetal hemoglobin Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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