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21111006: Complete trisomy 13 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
35482019 Complete trisomy 13 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
35483012 Patau syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
35484018 D>1< trisomy syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
750370014 Complete trisomy 13 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 13 syndrome Is a Anomaly of chromosome pair 13 false Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Is a Trisomy and partial trisomy of autosome false Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 1
Complete trisomy 13 syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Associated morphology Trisomy false Inferred relationship Existential restriction modifier 1
Complete trisomy 13 syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 2
Complete trisomy 13 syndrome Is a 13q partial trisomy syndrome false Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 2
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 1
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 2
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 1
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 1
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 2
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 1
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 2
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 2
Complete trisomy 13 syndrome Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 1
Complete trisomy 13 syndrome Is a Anomaly of chromosome pair 13 true Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Is a Trisomy and partial trisomy of autosome true Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Associated morphology Trisomy true Inferred relationship Existential restriction modifier 2
Complete trisomy 13 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Complete trisomy 13 syndrome Finding site Chromosome pair 13 true Inferred relationship Existential restriction modifier 1
Complete trisomy 13 syndrome Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Trisomy 13, meiotic nondisjunction Is a True Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier
Trisomy 13 - mitotic nondisjunction mosaicism Is a True Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier
Patau's syndrome NOS Is a False Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier
Aplasia cutis in Trisomy 13 syndrome Is a False Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier
Aplasia cutis in Trisomy 13 syndrome Associated with True Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier 2
Fetus with complete trisomy 13 syndrome Is a False Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier
Family history of trisomy 13 Associated finding True Complete trisomy 13 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 13 syndrome Inferred relationship Existential restriction modifier 3
Non-invasive prenatal testing for complete trisomy 13 syndrome screening (procedure) Has focus True Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier 1
Antenatal screening blood test for Down, Edwards and Patau syndromes (procedure) Has focus False Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier 3
Antenatal screening blood test for complete trisomy 18 and complete trisomy 13 syndromes (procedure) Has focus True Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier 2
Patau's syndrome NOS Is a False Complete trisomy 13 syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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