FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

64731000119106: Family history of multiple congenital anomalies (situation)

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

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 SNOMED CT core module
3467198016 Family history of multiple congenital anomalies en Synonym Active Entire term case insensitive SNOMED CT core module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of multiple congenital anomalies Is a Family history of congenital disease true Inferred relationship Existential restriction modifier
Family history of multiple congenital anomalies Associated finding Congenital malformation syndrome true Inferred relationship Existential restriction modifier 1
Family history of multiple congenital anomalies Finding context Known present true Inferred relationship Existential restriction modifier 1
Family history of multiple congenital anomalies Temporal context Current or past true Inferred relationship Existential restriction modifier 1
Family history of multiple congenital anomalies Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier 1
Family history of multiple congenital anomalies Is a Family history of development disorder true Inferred relationship Existential restriction modifier
Family history of multiple congenital anomalies Subject relationship context Person in the family true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of Steinert myotonic dystrophy Is a False Family history of multiple congenital anomalies Inferred relationship Existential restriction modifier
Family history of Prader-Willi syndrome Is a True Family history of multiple congenital anomalies Inferred relationship Existential restriction modifier
Family history of fragile X syndrome Is a True Family history of multiple congenital anomalies Inferred relationship Existential restriction modifier
Family history of Cowden syndrome Is a True Family history of multiple congenital anomalies Inferred relationship Existential restriction modifier
Family history of achondroplasia Is a True Family history of multiple congenital anomalies Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start