51053007: Hemoglobin C disease (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...

\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\hémoglobinose C (trouble)

\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\hémoglobinose C (trouble)
\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\hémoglobinose C (trouble)

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

1230942011 Homozygous for Hb C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

437441000241112 hémoglobinose C (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

495889019 Haemoglobin C disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

495890011 Haemoglobin C-C disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

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

85063019 Hemoglobin C disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

85064013 Hemoglobin C-C disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

966991000172111 hémoglobinose C fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
hémoglobinose C (trouble)	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
hémoglobinose C (trouble)	est un(e) (attribut)	Hereditary hemoglobinopathy due to globin chain mutation	true	Inferred relationship	Some
hémoglobinose C (trouble)	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
hémoglobinose C (trouble)	est défini par la manifestation de (attribut)	constatation à propos de la lignée rouge	false	Inferred relationship	Some
hémoglobinose C (trouble)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
hémoglobinose C (trouble)	localisation d'une constatation (attribut)	Erythrocyte	true	Inferred relationship	Some	1
hémoglobinose C (trouble)	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
hémoglobinose C (trouble)	localisation d'une constatation (attribut)	Erythrocyte	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hemoglobin C beta thalassemia (disorder)	est un(e) (attribut)	True	hémoglobinose C (trouble)	Inferred relationship	Some
Thalassemia-hemoglobin C disease	est un(e) (attribut)	True	hémoglobinose C (trouble)	Inferred relationship	Some

This concept is not in any reference sets