FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  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
2708385018 Family history of hereditary disease (situation) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character 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 Only initial character 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
402861000274117 Familienanamnese einer Erbkrankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5310761000241115 histoire familiale de maladie génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5310761000241115 histoire familiale de maladie génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
402861000274117 Familienanamnese einer Erbkrankheit de Synonym (core metadata concept) Active Entire term case sensitive (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
Family history of hereditary disease (situation) Is a Family history of disorder (situation) true Inferred relationship Existential restriction modifier (core metadata concept)
Family history of hereditary disease (situation) Finding context Known present (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Associated finding Hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Temporal context (attribute) Current or specified time (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Subject relationship context Person in the family false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Subject relationship context Person in the family true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Associated finding Hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Finding context Known present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Temporal context (attribute) Current or specified time (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Temporal context (attribute) Current or past (actual) (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Associated finding Hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Finding context Known present (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of hereditary disease (situation) Temporal context (attribute) Current or past (actual) (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of tuberous sclerosis (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Cholinesterase deficiency Is a False Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of sickle cell anemia Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Thalassemia Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Hereditary spherocytosis Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Sickle cell trait Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Charcot-Marie-Tooth disease Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Gout (situation) Is a False Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of alpha-1-antitrypsin deficiency Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of retinitis pigmentosa (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of familial multiple polyposis syndrome (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of familial dysautonomia Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of butyrylcholinesterase deficiency (situation) Is a False Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of glycogen storage disease (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of hereditary nonpolyposis colon cancer Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Marfan syndrome Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Tay-Sachs disease Is a False Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of phenylketonuria (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of neurofibromatosis (situation) Is a False Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Cowden syndrome Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of haemoglobinopathy E Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Von Hippel-Lindau syndrome (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of heritable malignancy (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of spinocerebellar ataxia (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of double heterozygous familial hypercholesterolemia Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Huntington's chorea (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of fragile X syndrome Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Cystic fibrosis Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of achondroplasia (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Steinert myotonic dystrophy (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of protein C resistance Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital long QT syndrome Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of lysosomal storage disease Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of spongy degeneration of central nervous system (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of hereditary diffuse carcinoma of stomach (situation) Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Rett syndrome Is a True Family history of hereditary disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start