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782880001: Hemoglobinopathy Toms River (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3756529010 Haemoglobinopathy Toms River en Synonym Active Only initial character case insensitive SNOMED CT core module
3756530017 Hemoglobinopathy Toms River (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3756531018 Hemoglobinopathy Toms River en Synonym Active Only initial character case insensitive SNOMED CT core module
3756532013 Transient neonatal cyanosis and anemia due to Toms River Hemoglobin en Synonym Active Only initial character case insensitive SNOMED CT core module
3756533015 Transient neonatal cyanosis and anaemia due to Toms River Haemoglobin en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hemoglobinopathy Toms River Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Hemoglobinopathy Toms River Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hemoglobinopathy Toms River Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1
Hemoglobinopathy Toms River Is a Hereditary hemoglobinopathy true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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