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205636003: monosomie van volledig chromosoom door meiotische non-disjunctie (aandoening)


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
315372014 Whole chromosome monosomy - meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591032017 Whole chromosome monosomy - meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
8757571000146117 monosomie van volledig chromosoom door meiotische non-disjunctie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8757581000146115 monosomie van volledig chromosoom door non-disjunctie tijdens meiose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8757591000146118 monosomie van volledig chromosoom door meiotische non-disjunctie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Whole chromosome monosomy - meiotic nondisjunction (disorder) Is a Monosomy and deletion from autosome (disorder) true Inferred relationship Some
Whole chromosome monosomy - meiotic nondisjunction (disorder) Occurrence Congenital false Inferred relationship Some
Whole chromosome monosomy - meiotic nondisjunction (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Some
Whole chromosome monosomy - meiotic nondisjunction (disorder) Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Finding site Chromosome structure false Inferred relationship Some 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some
Whole chromosome monosomy - meiotic nondisjunction (disorder) Finding site Chromosome structure false Inferred relationship Some 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Occurrence Congenital true Inferred relationship Some 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Some 1
Whole chromosome monosomy - meiotic nondisjunction (disorder) Finding site Chromosome true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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