123772008: Homozygous hemoglobinopathy (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy

\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy
\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy
\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy
\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy
\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy

\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

192261019 Homozygous hemoglobinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

203427013 Homozygous haemoglobinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

726889010 Homozygous hemoglobinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

819181000052118 homozygot hemoglobinopati sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous hemoglobinopathy	Is a	Hemoglobinopathy	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Finding site	Erythrocyte	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Is a	Hereditary hemoglobinopathy (disorder)	true	Inferred relationship	Some
Homozygous hemoglobinopathy	Finding site	Body system structure	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Occurrence	Congenital	true	Inferred relationship	Some	1
Homozygous hemoglobinopathy	Finding site	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-hemoglobin SS disease	Is a	True	Homozygous hemoglobinopathy	Inferred relationship	Some
Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)	Due to	True	Homozygous hemoglobinopathy	Inferred relationship	Some	2
Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)	Is a	True	Homozygous hemoglobinopathy	Inferred relationship	Some

This concept is not in any reference sets