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47461006: Genetic disorder carrier (finding)

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
494838011 Genetic disorder carrier en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
784922010 Genetic disorder carrier (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1230469015 Carrier of genetic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
494838011 Genetic disorder carrier en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494838011 Genetic disorder carrier en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
784922010 Genetic disorder carrier (finding) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
784922010 Genetic disorder carrier (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1230469015 Carrier of genetic disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1230469015 Carrier of genetic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4544971000241117 porteur d'une affection génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4544971000241117 porteur d'une affection génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

35 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Genetic disorder carrier Is a Carrier of disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Genetic disorder carrier Is a divers facteurs de risque pour le nouveau-né false Inferred relationship Existential restriction modifier (core metadata concept)
Genetic disorder carrier Is a Context-dependent finding false Inferred relationship Existential restriction modifier (core metadata concept)
Genetic disorder carrier Interprets General clinical state (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Genetic disorder carrier Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Genetic disorder carrier Is a Finding of lesion (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Genetic disorder carrier Is a constation sur l'état clinique général false Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of genetic disorder carrier (situation) Associated finding False Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of genetic disorder carrier (situation) Associated finding True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of genetic disorder carrier (situation) Associated finding False Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept) 1
Carrier of haemochromatosis Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of chromosome translocation (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of beta thalassemia (finding) Is a False Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of hemoglobinopathy C disorder Is a False Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of alpha thalassemia (finding) Is a False Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of hemoglobinopathy E disorder (finding) Is a False Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of fragile X chromosome Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of high risk cancer mutation gene (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of heritable cancer Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Duchenne muscular dystrophy (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Canavan disease (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of haemoglobinopathy disorder Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of familial dysautonomia (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of muscular dystrophy (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of von Willebrand disease (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of spinal muscular atrophy (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Bloom syndrome Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Cowden syndrome Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Gaucher disease (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Niemann-Pick disease type A (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Usher syndrome type 1F (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Usher syndrome type 3 (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Fanconi anemia group C Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Joubert syndrome with oculorenal defect (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Nebulin-related nemaline myopathy Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of mucolipidosis type IV (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Von Hippel-Lindau syndrome Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of familial hypercholesterolaemia Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of maple syrup urine disease type IB (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of dihydrolipoamide dehydrogenase deficiency (finding) Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of familial combined hyperlipidaemia Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of congenital cystic kidney disease Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of spinocerebellar ataxia Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)
Carrier of Usher syndrome type 2 Is a True Genetic disorder carrier Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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