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160417009: Family history of congenital disease (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
250089011 FH: Congenital anomaly en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
541328019 Family history: Congenital anomaly (context-dependent category) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2607185013 Family history: Congenital anomaly (situation) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2667855013 Family history: Congenital anomaly en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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
941191000195119 anamnesi familiare di malattia congenita it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
999331000241111 antécédents familiaux d'anomalie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
999341000241118 AF : anomalie congénitale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
999331000241111 antécédents familiaux d'anomalie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
999341000241118 AF : anomalie congénitale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
941191000195119 anamnesi familiare di malattia congenita it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

52 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of congenital disease (situation) Is a Family history of disorder (situation) true Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital disease (situation) Associated finding Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Subject relationship context Person in the family false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Temporal context (attribute) Current or specified time (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Finding context Known present (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Finding context Known present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Associated finding Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Temporal context (attribute) Current or specified time (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Subject relationship context Person in the family true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Temporal context (attribute) Current or past (actual) (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Associated finding Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Finding context Known present (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital disease (situation) Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of congenital 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 anencephaly Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Spina bifida (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Congenital RS anomaly Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital gastrointestinal tract anomaly (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital genitourinary anomaly (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Cong. orthopedic anomaly Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of chromosomal anomaly (situation) Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital CVS anomaly (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital anomaly NOS Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Gout (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Porphyria (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Hereditary spherocytosis Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital heart disease (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Polycystic kidney Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of hypertriglyceridemia Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of anencephaly Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital gastrointestinal tract anomaly (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital genitourinary anomaly (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of tuberous sclerosis (situation) Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital cataract (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of cleft lip Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of cleft palate (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of alpha-1-antitrypsin deficiency Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of cystic hygroma (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital hydrocephalus Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of macrocephaly (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of glycogen storage disease (situation) Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Tay-Sachs disease Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of phenylketonuria (situation) Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of neurofibromatosis (situation) Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of single congenital anomaly Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Cowden syndrome Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of multiple congenital anomalies (situation) Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Von Hippel-Lindau syndrome (situation) Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Thalassemia Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of sickle cell anemia Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
FH: Sickle cell trait Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of haemoglobinopathy E Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital microcephaly Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital immunodeficiency disease (situation) Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital long QT syndrome Is a False Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of lysosomal storage disease Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital malformation (situation) Is a True Family history of congenital disease (situation) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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