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205619006: Trisomy 13, meiotic nondisjunction (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Chromosomal disorder (disorder)\Autosomal chromosomal disorder (disorder)\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction (disorder)\Trisomy 13, meiotic nondisjunction
\Chromosomal disorder (disorder)\Autosomal chromosomal disorder (disorder)\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction
\Chromosomal disorder (disorder)\Duplication of chromosome\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction (disorder)\Trisomy 13, meiotic nondisjunction
\Chromosomal disorder (disorder)\Duplication of chromosome\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction
\Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 13\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction
\Chromosomal disorder (disorder)\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction (disorder)\Trisomy 13, meiotic nondisjunction
\Chromosomal disorder (disorder)\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction

\Congenital disease (disorder)\Congenital malformation\Trisomy 13, meiotic nondisjunction
\Congenital disease (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 13\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction
\Congenital disease (disorder)\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction (disorder)\Trisomy 13, meiotic nondisjunction
\Congenital disease (disorder)\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction

\Developmental disorder\Congenital malformation\Trisomy 13, meiotic nondisjunction

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

Descriptions:

Id Description Lang Type Status Case? Module

315350012 Trisomy 13, meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591013011 Trisomy 13, meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2479111000052113 trisomi 13, meiotisk icke-disjunktion sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Trisomy 13, meiotic nondisjunction	Is a	Complete trisomy 13 syndrome	true	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	Occurrence	Congenital	false	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	Associated morphology	Trisomy	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	Finding site	Sex chromosome	false	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Associated morphology	kongenital anomali	false	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	Associated morphology	Trisomy	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	Occurrence	Congenital	true	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Finding site	Chromosome pair 13	true	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Associated morphology	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Is a	Whole chromosome trisomy meiotic nondisjunction (disorder)	true	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	Is a	Congenital malformation	true	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	Associated morphology	Trisomy	true	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1

Inbound Relationships

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Active

Source

Characteristic

Refinability

Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
315350012	Trisomy 13, meiotic nondisjunction	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
591013011	Trisomy 13, meiotic nondisjunction (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2479111000052113	trisomi 13, meiotisk icke-disjunktion	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)