205634000: Deletion seen only at prometaphase (disorder)

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

\Disorder of foetus and/or newborn\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Monosomy and deletion from autosome (disorder)\Deletion seen only at prometaphase

\Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Monosomy and deletion from autosome (disorder)\Deletion seen only at prometaphase

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

315370018 Deletion seen only at prometaphase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

591030013 Deletion seen only at prometaphase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

315370018 Deletion seen only at prometaphase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

315370018 Deletion seen only at prometaphase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

591030013 Deletion seen only at prometaphase (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

591030013 Deletion seen only at prometaphase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4885881000241119 délétion vue uniquement à la prométaphase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4885881000241119 délétion vue uniquement à la prométaphase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Deletion seen only at prometaphase	Is a	Monosomy and deletion from autosome (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion seen only at prometaphase	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion seen only at prometaphase	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion seen only at prometaphase	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion seen only at prometaphase	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion seen only at prometaphase	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion seen only at prometaphase	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion seen only at prometaphase	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion seen only at prometaphase	Associated morphology	Cellular AND/OR subcellular abnormality	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Deletion seen only at prometaphase	Finding site	Chromosome	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Description inactivation indicator reference set