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427306008: Hereditary hemoglobinopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2007. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2662307010 Hereditary hemoglobinopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2674112019 Hereditary hemoglobinopathy en Synonym Active Entire term case insensitive SNOMED CT core module
2674113012 Hereditary haemoglobinopathy en Synonym Active Entire term case insensitive SNOMED CT core module


118 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary hemoglobinopathy Is a Hemoglobinopathy true Inferred relationship Existential restriction modifier
Hereditary hemoglobinopathy Is a Hereditary red blood cell disorder true Inferred relationship Existential restriction modifier
Hereditary hemoglobinopathy Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary hemoglobinopathy Has definitional manifestation Red blood cell finding false Inferred relationship Existential restriction modifier
Hereditary hemoglobinopathy Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Hereditary hemoglobinopathy Is a Congenital disease true Inferred relationship Existential restriction modifier
Hereditary hemoglobinopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hereditary hemoglobinopathy Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Homozygous hemoglobinopathy Is a True Hereditary hemoglobinopathy Inferred relationship Existential restriction modifier
Thalassemia Is a True Hereditary hemoglobinopathy Inferred relationship Existential restriction modifier
Hereditary hemoglobinopathy due to globin chain mutation Is a True Hereditary hemoglobinopathy Inferred relationship Existential restriction modifier
Hereditary persistence of fetal hemoglobin Is a True Hereditary hemoglobinopathy Inferred relationship Existential restriction modifier
Heterozygous hemoglobinopathy Is a True Hereditary hemoglobinopathy Inferred relationship Existential restriction modifier
Hemoglobinopathy Toms River Is a True Hereditary hemoglobinopathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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