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64731000119106: Family history of multiple congenital anomalies (situation)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3467197014 Family history of multiple congenital anomalies (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3467198016 Family history of multiple congenital anomalies en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5307141000172113 congenitaal malformatiesyndroom in familieanamnese nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of multiple congenital anomalies (situation) Is a Family history of congenital disease (situation) true Inferred relationship Some
Family history of multiple congenital anomalies (situation) Associated finding Congenital malformation syndrome (disorder) true Inferred relationship Some 1
Family history of multiple congenital anomalies (situation) Finding context (attribute) Known present (qualifier value) true Inferred relationship Some 1
Family history of multiple congenital anomalies (situation) Temporal context (attribute) Current or past (actual) (qualifier value) true Inferred relationship Some 1
Family history of multiple congenital anomalies (situation) Subject relationship context (attribute) persoon in familie van zorgafnemer false Inferred relationship Some 1
Family history of multiple congenital anomalies (situation) Is a Family history of development disorder true Inferred relationship Some
Family history of multiple congenital anomalies (situation) Subject relationship context (attribute) Person in the family (person) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of Steinert myotonic dystrophy (situation) Is a False Family history of multiple congenital anomalies (situation) Inferred relationship Some
Family history of Prader-Willi syndrome Is a True Family history of multiple congenital anomalies (situation) Inferred relationship Some
Family history of fragile X syndrome (situation) Is a True Family history of multiple congenital anomalies (situation) Inferred relationship Some
Family history of Cowden syndrome (situation) Is a True Family history of multiple congenital anomalies (situation) Inferred relationship Some
Family history of achondroplasia (situation) Is a True Family history of multiple congenital anomalies (situation) Inferred relationship Some

Reference Sets

GB English

US English

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