205645002: Other condition due to autosomal anomaly (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

315387016 Other condition due to autosomal anomaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

591042015 Other condition due to autosomal anomaly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

315387016 Other condition due to autosomal anomaly en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

315387016 Other condition due to autosomal anomaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

591042015 Other condition due to autosomal anomaly (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

591042015 Other condition due to autosomal anomaly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Other condition due to autosomal anomaly	Is a	Congenital chromosomal disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Other condition due to autosomal anomaly	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Other condition due to autosomal anomaly	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Other condition due to autosomal anomaly	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other condition due to autosomal anomaly	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other condition due to autosomal anomaly	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Other condition due to autosomal anomaly	Finding site	Chromosome structure (cell structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Conditions due to anomaly of unspecified chromosome NOS	Is a	False	Other condition due to autosomal anomaly	Inferred relationship	Existential restriction modifier (core metadata concept)
Other specified conditions due to autosomal anomalies	Is a	False	Other condition due to autosomal anomaly	Inferred relationship	Existential restriction modifier (core metadata concept)
Unspecified conditions due to autosomal anomalies	Is a	False	Other condition due to autosomal anomaly	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

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

WAS A association reference set (foundation metadata concept)