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66751000119109: Carrier of hemoglobinopathy disorder (finding)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3515927010 Carrier of hemoglobinopathy disorder (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3515928017 Carrier of hemoglobinopathy disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3516793019 Carrier of haemoglobinopathy disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3515927010 Carrier of hemoglobinopathy disorder (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3515928017 Carrier of hemoglobinopathy disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3516793019 Carrier of haemoglobinopathy disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5798311000241119 porteur d'une hémoglobinopathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5798311000241119 porteur d'une hémoglobinopathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Carrier of haemoglobinopathy disorder Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of haemoglobinopathy disorder Is a Genetic disorder carrier true Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of haemoglobinopathy disorder Interprets General clinical state (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Carrier of haemoglobinopathy disorder Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Carrier of beta thalassemia (finding) Is a True Carrier of haemoglobinopathy disorder Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of hemoglobinopathy C disorder Is a True Carrier of haemoglobinopathy disorder Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of alpha thalassemia (finding) Is a True Carrier of haemoglobinopathy disorder Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of hemoglobinopathy E disorder (finding) Is a True Carrier of haemoglobinopathy disorder Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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