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205623003: Trisomy 18 - meiotic nondisjunction (disorder)

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
315354015 Trisomy 18 - meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591018019 Trisomy 18 - meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
315354015 Trisomy 18 - meiotic nondisjunction en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315354015 Trisomy 18 - meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591018019 Trisomy 18 - meiotic nondisjunction (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591018019 Trisomy 18 - meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4885801000241113 trisomie 18 sans disjonction méiotique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4885801000241113 trisomie 18 sans disjonction méiotique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Trisomy 18 - meiotic nondisjunction (disorder) Is a Complete trisomy 18 syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 18 - meiotic nondisjunction (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 18 - meiotic nondisjunction (disorder) Associated morphology Trisomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 18 - meiotic nondisjunction (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 false Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 18 - meiotic nondisjunction (disorder) Associated morphology Trisomy (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Trisomy 18 - meiotic nondisjunction (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 18 - meiotic nondisjunction (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Finding site Chromosome pair 18 true Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 18 - meiotic nondisjunction (disorder) Is a Whole chromosome trisomy meiotic nondisjunction (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 18 - meiotic nondisjunction (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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