205656002: Whole chromosome trisomy, meiotic nondisjunction (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2718984015 Whole chromosome trisomy, meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2770276013 Whole chromosome trisomy, meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

315398015 Whole chromosome trisomy, meitotic nondisjunction en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

591054015 Whole chromosome trisomy, meitotic nondisjunction (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2718984015 Whole chromosome trisomy, meiotic nondisjunction (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2718984015 Whole chromosome trisomy, meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2770276013 Whole chromosome trisomy, meiotic nondisjunction en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2770276013 Whole chromosome trisomy, meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Whole chromosome trisomy, meitotic nondisjunction	Is a	Trisomy and partial trisomy of autosome	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Whole chromosome trisomy, meitotic nondisjunction	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Whole chromosome trisomy, meitotic nondisjunction	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Whole chromosome trisomy, meitotic nondisjunction	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Whole chromosome trisomy, meitotic nondisjunction	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Whole chromosome trisomy, meitotic nondisjunction	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Whole chromosome trisomy, meitotic nondisjunction	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Whole chromosome trisomy, meitotic nondisjunction	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Whole chromosome trisomy, meitotic nondisjunction	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Whole chromosome trisomy, meitotic nondisjunction	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

SAME AS association reference set (foundation metadata concept)