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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
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

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) false Inferred relationship Existential restriction modifier (core metadata concept)
Family history of multiple congenital anomalies (situation) Associated finding Congenital malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of multiple congenital anomalies (situation) Finding context Known present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of multiple congenital anomalies (situation) Temporal context (attribute) Current or past (actual) (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of multiple congenital anomalies (situation) Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of multiple congenital anomalies (situation) Is a Family history of development disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Family history of multiple congenital anomalies (situation) Subject relationship context Person in the family true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of multiple congenital anomalies (situation) Is a Family history of congenital malformation (situation) true Inferred relationship Existential restriction modifier (core metadata concept)
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 Existential restriction modifier (core metadata concept)
Family history of Prader-Willi syndrome Is a True Family history of multiple congenital anomalies (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of fragile X syndrome Is a True Family history of multiple congenital anomalies (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of Cowden syndrome Is a True Family history of multiple congenital anomalies (situation) Inferred relationship Existential restriction modifier (core metadata concept)
Family history of achondroplasia (situation) Is a True Family history of multiple congenital anomalies (situation) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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