51053007: Hemoglobin C disease (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 C disease

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease

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

85063019 Hemoglobin C disease en Synonym Active Entire term case sensitive SNOMED CT core module

85064013 Hemoglobin C-C disease en Synonym Active Entire term case sensitive SNOMED CT core module

495889019 Haemoglobin C disease en Synonym Active Only initial character case insensitive SNOMED CT core module

495890011 Haemoglobin C-C disease en Synonym Active Only initial character case insensitive SNOMED CT core module

788910019 Hemoglobin C disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

1230942011 Homozygous for Hb C en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Thalassemia-hemoglobin C disease	Is a	True	Hemoglobin C disease	Inferred relationship	Existential restriction modifier
Hemoglobin C beta thalassemia	Is a	True	Hemoglobin C disease	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets