7391009: Hemoglobin D trait (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\...

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\...

\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin D trait

\Heterozygous hemoglobinopathy\Hemoglobin D trait

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin D trait
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin D trait
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin D trait
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin D trait

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

13181013 Hemoglobin D trait en Synonym Active Entire term case sensitive SNOMED CT core module

13182018 Hemoglobin D-A disorder en Synonym Active Entire term case sensitive SNOMED CT core module

502562017 Heterozygous for Hb D en Synonym Active Only initial character case insensitive SNOMED CT core module

502563010 Haemoglobin D-A disorder en Synonym Active Entire term case sensitive SNOMED CT core module

502564016 Haemoglobin D trait en Synonym Active Entire term case sensitive SNOMED CT core module

814351014 Hemoglobin D trait (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemoglobin D trait	Is a	Hereditary hemoglobinopathy due to globin chain mutation	true	Inferred relationship	Existential restriction modifier
Hemoglobin D trait	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hemoglobin D trait	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Hemoglobin D trait	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hemoglobin D trait	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Existential restriction modifier
Hemoglobin D trait	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hemoglobin D trait	Is a	Heterozygous hemoglobinopathy	true	Inferred relationship	Existential restriction modifier
Hemoglobin D trait	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Hemoglobin D 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 D carrier (situation)	Associated finding	True	Hemoglobin D trait	Inferred relationship	Existential restriction modifier	1
Result consistent with haemoglobin D carrier	Associated finding	True	Hemoglobin D trait	Inferred relationship	Existential restriction modifier	1

This concept is not in any reference sets