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205638002: Monosomy 21, mosaicism (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
315377015 Monosomy 21, mosaicism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591035015 Monosomy 21, mosaicism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
315377015 Monosomy 21, mosaicism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315377015 Monosomy 21, mosaicism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591035015 Monosomy 21, mosaicism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591035015 Monosomy 21, mosaicism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4885921000241114 monosomie 21, mosaïcisme fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4885921000241114 monosomie 21, mosaïcisme 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
Monosomy 21, mosaicism (disorder) Is a Monosomy and deletion from autosome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Monosomy 21, mosaicism (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Monosomy 21, mosaicism (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Monosomy 21, mosaicism (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Monosomy 21, mosaicism (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Monosomy 21, mosaicism (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Monosomy 21, mosaicism (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Monosomy 21, mosaicism (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Monosomy 21, mosaicism (disorder) Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier (core metadata concept) 1
Monosomy 21, mosaicism (disorder) Finding site Chromosome 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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