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160417009: antécédents familiaux d'anomalie congénitale (situation)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4546425019 Family history of congenital anomaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4546426018 Family history of congenital disease (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4546427010 Family history of congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
999321000241114 antécédents familiaux d'anomalie congénitale (situation) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
999331000241111 antécédents familiaux d'anomalie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
999341000241118 AF : anomalie congénitale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


50 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of congenital microcephaly est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of congenital immunodeficiency disease (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
FH: Gout est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
FH: Porphyria est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
FH: Hereditary spherocytosis est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
FH: Congenital heart disease est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
FH: Polycystic kidney est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history: Triglyceride high (situation) est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
Family history: Anencephaly (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
FH: Congenital GIT anomaly est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
FH: Congenital GU anomaly est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of tuberous sclerosis est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history: Anencephaly (situation) est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
Family history: Spina bifida (situation) est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
FH: Congenital RS anomaly est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
FH: Congenital GIT anomaly est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
FH: Congenital GU anomaly est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
FH: Cong. orthopedic anomaly est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of chromosomal anomaly (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of congenital cataract (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of cleft lip (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of cleft palate (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of alpha-1-antitrypsin deficiency (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of congenital anomaly of cardiovascular system est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
FH: Congenital anomaly NOS est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
Family history of cystic hygroma est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of congenital hydrocephalus est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of macrocephaly est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
Family history of glycogen storage disease (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of Tay-Sachs disease est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of phenylketonuria est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of neurofibromatosis (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of single congenital anomaly est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of Cowden syndrome (situation) est un(e) (attribut) False Family history of congenital disease (situation) Inferred relationship Some
Family history of multiple congenital anomalies (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of Von Hippel-Lindau syndrome (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
FH: Thalassemia est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of sickle cell anaemia est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
FH: Sickle cell trait est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some
Family history of hemoglobinopathy E (situation) est un(e) (attribut) True Family history of congenital disease (situation) Inferred relationship Some

This concept is not in any reference sets

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