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76050008: Hemoglobin C trait (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
126315012 Hemoglobin C trait en Synonym Active Entire term case sensitive SNOMED CT core module
126316013 Hemoglobin C-A disorder en Synonym Active Entire term case sensitive SNOMED CT core module
503177011 Heterozygous for Hb C en Synonym Active Only initial character case insensitive SNOMED CT core module
503178018 Haemoglobin C trait en Synonym Active Entire term case sensitive SNOMED CT core module
503179014 Haemoglobin C-A disorder en Synonym Active Entire term case sensitive SNOMED CT core module
816728014 Hemoglobin C trait (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hemoglobin C trait Is a Hereditary hemoglobinopathy due to globin chain mutation true Inferred relationship Existential restriction modifier
Hemoglobin C trait Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hemoglobin C trait Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Hemoglobin C trait Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hemoglobin C trait Finding site Body system structure false Inferred relationship Existential restriction modifier
Hemoglobin C trait Has definitional manifestation Red blood cell finding false Inferred relationship Existential restriction modifier
Hemoglobin C trait Is a Heterozygous hemoglobinopathy true Inferred relationship Existential restriction modifier
Hemoglobin C trait Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hemoglobin C trait Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
National Health Service Sickle Cell and Thalassaemia Screening Programme result consistent with Haemoglobin C carrier (situation) Associated finding True Hemoglobin C trait Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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