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427306008: Hereditary hemoglobinopathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2007. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2662307010 Hereditary hemoglobinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2674112019 Hereditary hemoglobinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2674113012 Hereditary haemoglobinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2662307010 Hereditary hemoglobinopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2662307010 Hereditary hemoglobinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2674112019 Hereditary hemoglobinopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2674112019 Hereditary hemoglobinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2674113012 Hereditary haemoglobinopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2674113012 Hereditary haemoglobinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5301661000241117 hémoglobinopathie héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5301661000241117 hémoglobinopathie héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

123 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary hemoglobinopathy (disorder) Is a Haemoglobinopathy true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary hemoglobinopathy (disorder) Is a Hereditary red blood cell disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary hemoglobinopathy (disorder) Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary hemoglobinopathy (disorder) Has definitional manifestation Red blood cell finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary hemoglobinopathy (disorder) Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary hemoglobinopathy (disorder) Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary hemoglobinopathy (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary hemoglobinopathy (disorder) Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Homozygous haemoglobinopathy Is a True Hereditary hemoglobinopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Thalassaemia Is a True Hereditary hemoglobinopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary hemoglobinopathy due to globin chain mutation Is a True Hereditary hemoglobinopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary persistence of fetal hemoglobin Is a True Hereditary hemoglobinopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Heterozygous hemoglobinopathy (disorder) Is a True Hereditary hemoglobinopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Haemoglobinopathy Toms River Is a True Hereditary hemoglobinopathy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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