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44621005: Congenital anomaly of organ of Corti (disorder)


Status: current, 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
74440018 Congenital anomaly of organ of Corti en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
493956018 Congenital anomaly of the organ of Corti en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
781771014 Congenital anomaly of organ of Corti (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
74440018 Congenital anomaly of organ of Corti en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
493956018 Congenital anomaly of the organ of Corti en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
781771014 Congenital anomaly of organ of Corti (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5889961000241113 anomalie congénitale de l'organe de Corti fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5889971000241117 anomalie congénitale de l'organe spiral fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5889961000241113 anomalie congénitale de l'organe de Corti fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5889971000241117 anomalie congénitale de l'organe spiral 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
Congenital anomaly of organ of Corti Is a Disorder of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Is a Congenital abnormal shape of inner ear false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Associated morphology Congenital abnormal shape false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Finding site Organ of Corti structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of organ of Corti Is a Disease of skull false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Is a Congenital anomaly of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Is a Congenital anomaly of membranous labyrinth (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Is a Congenital anomaly of skull false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Is a Congenital anomaly of nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of organ of Corti Is a Congenital anomaly of central nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Is a Congenital anomaly of skeletal bone false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Is a Congenital anomaly of skull true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of organ of Corti Finding site Organ of Corti structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of organ of Corti Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of organ of Corti Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of organ of Corti Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of organ of Corti Finding site Organ of Corti structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of organ of Corti Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of organ of Corti Finding site Organ of Corti structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of organ of Corti Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of organ of Corti Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of organ of Corti Is a Congenital anomaly of cochlea (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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