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51500006: Complete trisomy 18 syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
85775018 Complete trisomy 18 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
85776017 Edwards syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
789405015 Complete trisomy 18 syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complete trisomy 18 syndrome Is a Anomaly of chromosome pair 18 true Inferred relationship Existential restriction modifier
Complete trisomy 18 syndrome Is a Trisomy and partial trisomy of autosome true Inferred relationship Existential restriction modifier
Complete trisomy 18 syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Complete trisomy 18 syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Complete trisomy 18 syndrome Associated morphology Trisomy true Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 2
Complete trisomy 18 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 2
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 2
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 2
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 2
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 2
Complete trisomy 18 syndrome Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Associated morphology Trisomy false Inferred relationship Existential restriction modifier 2
Complete trisomy 18 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Complete trisomy 18 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Finding site Chromosome pair 18 true Inferred relationship Existential restriction modifier 1
Complete trisomy 18 syndrome Is a Congenital malformation true Inferred relationship Existential restriction modifier
Complete trisomy 18 syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Trisomy 18 - meiotic nondisjunction Is a True Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier
Trisomy 18 - mitotic nondisjunction mosaicism Is a True Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier
Edward's syndrome NOS Is a False Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier
Fetus with complete trisomy 18 syndrome Is a False Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier
Family history of trisomy 18 Associated finding True Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier 1
Antenatal screening blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes (procedure) Has focus True Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier 2
Non-invasive prenatal testing for complete trisomy 18 syndrome screening (procedure) Has focus True Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier 1
Antenatal screening blood test for Down, Edwards and Patau syndromes (procedure) Has focus False Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier 2
Antenatal screening blood test for complete trisomy 18 and complete trisomy 13 syndromes (procedure) Has focus True Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier 1
Edward's syndrome NOS Is a False Complete trisomy 18 syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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