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123772008: Homozygous hemoglobinopathy (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
192261019 Homozygous hemoglobinopathy en Synonym Active Entire term case insensitive SNOMED CT core module
203427013 Homozygous haemoglobinopathy en Synonym Active Entire term case insensitive SNOMED CT core module
726889010 Homozygous hemoglobinopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

11 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homozygous hemoglobinopathy Is a Hemoglobinopathy false Inferred relationship Existential restriction modifier
Homozygous hemoglobinopathy Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Homozygous hemoglobinopathy Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Homozygous hemoglobinopathy Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Homozygous hemoglobinopathy Has definitional manifestation Red blood cell finding false Inferred relationship Existential restriction modifier
Homozygous hemoglobinopathy Is a Hereditary hemoglobinopathy true Inferred relationship Existential restriction modifier
Homozygous hemoglobinopathy Finding site Body system structure false Inferred relationship Existential restriction modifier
Homozygous hemoglobinopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Homozygous hemoglobinopathy Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Sickle cell-hemoglobin SS disease Is a True Homozygous hemoglobinopathy Inferred relationship Existential restriction modifier
Vaso-occlusive pain co-occurrent and due to sickle cell disease Due to True Homozygous hemoglobinopathy Inferred relationship Existential restriction modifier 2
Vaso-occlusive pain co-occurrent and due to sickle cell disease Is a True Homozygous hemoglobinopathy Inferred relationship Existential restriction modifier
National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant not clinically significant (situation) Associated finding True Homozygous hemoglobinopathy Inferred relationship Existential restriction modifier 1
National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant clinically significant (situation) Associated finding True Homozygous hemoglobinopathy Inferred relationship Existential restriction modifier 1
National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant of unknown clinical significance (situation) Associated finding True Homozygous hemoglobinopathy Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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