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160425006: Family history of chromosomal anomaly (situation)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
250101013 FH: Chromosomal anomaly en Synonym Inactive Entire term case sensitive SNOMED CT core module
541336011 Family history: Chromosomal anomaly (context-dependent category) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
2607192015 Family history: Chromosomal anomaly (situation) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
2667268014 Family history: Chromosomal anomaly en Synonym Inactive Only initial character case insensitive SNOMED CT core module
4546423014 Family history of chromosomal anomaly (situation) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4546424015 Family history of chromosomal anomaly en Synonym Active Entire term case insensitive SNOMED CT core module

7 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of chromosomal anomaly Is a Family history of congenital disease true Inferred relationship Existential restriction modifier
Family history of chromosomal anomaly Associated finding Congenital disorder due to abnormality of chromosome number OR structure false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Finding context Known present false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Temporal context Current or specified time false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Subject relationship context Person in the family false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Finding context Known present true Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Temporal context Current or specified time false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Associated finding Congenital disorder due to abnormality of chromosome number OR structure true Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Subject relationship context Person in the family true Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Temporal context Current or past false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Associated finding Congenital disorder due to abnormality of chromosome number OR structure false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Finding context Known present false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Subject relationship context Person in family of subject false Inferred relationship Existential restriction modifier 1
Family history of chromosomal anomaly Temporal context Current or past true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of complete trisomy 21 syndrome Is a True Family history of chromosomal anomaly Inferred relationship Existential restriction modifier
Family history of Prader-Willi syndrome Is a False Family history of chromosomal anomaly Inferred relationship Existential restriction modifier
Family history of fragile X syndrome Is a True Family history of chromosomal anomaly Inferred relationship Existential restriction modifier
Family history of trisomy 13 Is a True Family history of chromosomal anomaly Inferred relationship Existential restriction modifier
Family history of trisomy 18 Is a True Family history of chromosomal anomaly Inferred relationship Existential restriction modifier
Family history of Turner syndrome Is a True Family history of chromosomal anomaly Inferred relationship Existential restriction modifier
Family history of sex chromosome aneuploidy Is a True Family history of chromosomal anomaly Inferred relationship Existential restriction modifier
Family history of fragile X syndrome in first degree relative Is a True Family history of chromosomal anomaly Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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