FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

429962007: Family history of hereditary disease (situation)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2008. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2708385018 Family history of hereditary disease (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2764084012 Family history of genetic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2764338014 Family history of hereditary disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3035781016 Family history of heritable disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


30 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of hereditary disease (situation) est un(e) (attribut) antécédents familiaux de troubles true Inferred relationship Some
Family history of hereditary disease (situation) contexte de la constatation (attribut) présence connue false Inferred relationship Some 1
Family history of hereditary disease (situation) constatation associée (attribut) maladie héréditaire false Inferred relationship Some 1
Family history of hereditary disease (situation) contexte temporel (attribut) Current or specified time (qualifier value) false Inferred relationship Some 1
Family history of hereditary disease (situation) nature de la relation avec la personne visée (attribut) membre de la famille false Inferred relationship Some 1
Family history of hereditary disease (situation) nature de la relation avec la personne visée (attribut) membre de la famille false Inferred relationship Some 1
Family history of hereditary disease (situation) constatation associée (attribut) maladie héréditaire true Inferred relationship Some 1
Family history of hereditary disease (situation) contexte de la constatation (attribut) présence connue true Inferred relationship Some 1
Family history of hereditary disease (situation) contexte temporel (attribut) Current or specified time (qualifier value) false Inferred relationship Some 1
Family history of hereditary disease (situation) contexte temporel (attribut) actuel ou passé false Inferred relationship Some 1
Family history of hereditary disease (situation) constatation associée (attribut) maladie héréditaire false Inferred relationship Some 1
Family history of hereditary disease (situation) contexte de la constatation (attribut) présence connue false Inferred relationship Some 1
Family history of hereditary disease (situation) nature de la relation avec la personne visée (attribut) Person in family of subject (person) false Inferred relationship Some 1
Family history of hereditary disease (situation) nature de la relation avec la personne visée (attribut) Person in family of subject (person) true Inferred relationship Some 1
Family history of hereditary disease (situation) contexte temporel (attribut) actuel ou passé true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
FH: Huntington's chorea est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of fragile X syndrome (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of cystic fibrosis (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of achondroplasia (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of Steinert myotonic dystrophy (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of protein C resistance (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of tuberous sclerosis est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
FH: Cholinesterase deficiency est un(e) (attribut) False Family history of hereditary disease (situation) Inferred relationship Some
Family history of sickle cell anaemia est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
FH: Thalassemia est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
FH: Hereditary spherocytosis est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
FH: Sickle cell trait est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of Charcot-Marie-Tooth disease (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
FH: Gout est un(e) (attribut) False Family history of hereditary disease (situation) Inferred relationship Some
Family history of alpha-1-antitrypsin deficiency (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of retinitis pigmentosa (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of familial multiple polyposis syndrome (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of familial dysautonomia est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of butyrylcholinesterase deficiency est un(e) (attribut) False Family history of hereditary disease (situation) Inferred relationship Some
Family history of glycogen storage disease (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of hereditary nonpolyposis colon cancer est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of Marfan syndrome (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of Tay-Sachs disease est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of phenylketonuria est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of neurofibromatosis (situation) est un(e) (attribut) False Family history of hereditary disease (situation) Inferred relationship Some
Family history of Cowden syndrome (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of hemoglobinopathy E (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of Von Hippel-Lindau syndrome (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of heritable malignancy (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of spinocerebellar ataxia (situation) est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some
Family history of double heterozygous familial hypercholesterolaemia est un(e) (attribut) True Family history of hereditary disease (situation) Inferred relationship Some

This concept is not in any reference sets

Back to Start