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66751000119109: Carrier of hemoglobinopathy disorder (finding)


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

Descriptions:

Id Description Lang Type Status Case? Module
3515927010 Carrier of hemoglobinopathy disorder (finding) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3515928017 Carrier of hemoglobinopathy disorder en Synonym Active Entire term case insensitive SNOMED CT core module
3516793019 Carrier of haemoglobinopathy disorder en Synonym Active Entire term case insensitive SNOMED CT core module


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Carrier of hemoglobinopathy disorder Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Carrier of hemoglobinopathy disorder Is a Genetic disorder carrier true Inferred relationship Existential restriction modifier
Carrier of hemoglobinopathy disorder Interprets General clinical state true Inferred relationship Existential restriction modifier 2
Carrier of hemoglobinopathy disorder Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Carrier of beta thalassemia Is a True Carrier of hemoglobinopathy disorder Inferred relationship Existential restriction modifier
Carrier of hemoglobinopathy C disorder Is a True Carrier of hemoglobinopathy disorder Inferred relationship Existential restriction modifier
Carrier of alpha thalassemia Is a True Carrier of hemoglobinopathy disorder Inferred relationship Existential restriction modifier
Carrier of hemoglobinopathy E disorder Is a True Carrier of hemoglobinopathy disorder Inferred relationship Existential restriction modifier
Carrier of delta-beta thalassaemia disorder Is a True Carrier of hemoglobinopathy disorder Inferred relationship Existential restriction modifier
National Health Service Sickle Cell and Thalassaemia Screening Programme result consistent with hereditary persistence of fetal haemoglobin carrier (situation) Associated finding True Carrier of hemoglobinopathy disorder Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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