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412749001: antécédents familiaux de trouble du développement (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
2474306014 Family history of development disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2478435012 FH: Development disorder en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2613160014 Family history of development disorder (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3387370016 antécédents familiaux de trouble du développement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
644681000241112 antécédents familiaux de trouble du développement (situation) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

43 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of development disorder est un(e) (attribut) antécédents familiaux de troubles true Inferred relationship Some
Family history of development disorder contexte de la constatation (attribut) présence connue false Inferred relationship Some 1
Family history of development disorder constatation associée (attribut) trouble du développement false Inferred relationship Some 1
Family history of development disorder nature de la relation avec la personne visée (attribut) membre de la famille false Inferred relationship Some 2
Family history of development disorder nature de la relation avec la personne visée (attribut) membre de la famille false Inferred relationship Some 1
Family history of development disorder contexte temporel (attribut) Current or specified time (qualifier value) false Inferred relationship Some 1
Family history of development disorder constatation associée (attribut) Disease false Inferred relationship Some 2
Family history of development disorder nature de la relation avec la personne visée (attribut) membre de la famille false Inferred relationship Some 1
Family history of development disorder nature de la relation avec la personne visée (attribut) membre de la famille false Inferred relationship Some 2
Family history of development disorder contexte de la constatation (attribut) présence connue true Inferred relationship Some 1
Family history of development disorder constatation associée (attribut) trouble du développement true Inferred relationship Some 1
Family history of development disorder nature de la relation avec la personne visée (attribut) membre de la famille false Inferred relationship Some 1
Family history of development disorder contexte temporel (attribut) Current or specified time (qualifier value) false Inferred relationship Some 1
Family history of development disorder nature de la relation avec la personne visée (attribut) Person in family of subject (person) false Inferred relationship Some 1
Family history of development disorder contexte de la constatation (attribut) présence connue false Inferred relationship Some 1
Family history of development disorder constatation associée (attribut) trouble du développement false Inferred relationship Some 1
Family history of development disorder contexte temporel (attribut) actuel ou passé false Inferred relationship Some 1
Family history of development disorder contexte temporel (attribut) actuel ou passé true Inferred relationship Some 1
Family history of development disorder nature de la relation avec la personne visée (attribut) Person in family of subject (person) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
FH: Congenital GIT anomaly est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of cleft palate (situation) est un(e) (attribut) True Family history of development disorder Inferred relationship Some
FH: Muscular dystrophy est un(e) (attribut) True Family history of development disorder Inferred relationship Some
FH: Cong. orthopedic anomaly est un(e) (attribut) True Family history of development disorder Inferred relationship Some
FH: Congenital GU anomaly est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of congenital anomaly of cardiovascular system est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of single congenital anomaly est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history: Anencephaly (situation) est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of congenital cataract (situation) est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of congenital hydrocephalus est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of neurofibromatosis (situation) est un(e) (attribut) False Family history of development disorder Inferred relationship Some
Family history of Von Hippel-Lindau syndrome (situation) est un(e) (attribut) False Family history of development disorder Inferred relationship Some
Family history of macrocephaly est un(e) (attribut) False Family history of development disorder Inferred relationship Some
Family history of cleft lip (situation) est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of cystic hygroma est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of tuberous sclerosis est un(e) (attribut) False Family history of development disorder Inferred relationship Some
FH: Congenital RS anomaly est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of multiple congenital anomalies (situation) est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of congenital microcephaly est un(e) (attribut) True Family history of development disorder Inferred relationship Some
antécédents familiaux de trisomie 21 complète est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of trisomy 18 (situation) est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of mental retardation (situation) est un(e) (attribut) False Family history of development disorder Inferred relationship Some
Family history of learning disability (situation) est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of autism est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of speech and language disorder (situation) est un(e) (attribut) False Family history of development disorder Inferred relationship Some
Family history of attention deficit hyperactivity disorder (situation) est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of short stature est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of neurological developmental delay est un(e) (attribut) True Family history of development disorder Inferred relationship Some
Family history of intellectual disability est un(e) (attribut) True Family history of development disorder Inferred relationship Some

This concept is not in any reference sets

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