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737344003: Congenital conductive hearing loss (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3527478013 Congenital conductive hearing loss en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3527479017 Congenital conductive hearing loss (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3527478013 Congenital conductive hearing loss en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3527479017 Congenital conductive hearing loss (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5946841000241114 surdité congénitale de transmission fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5946851000241112 perte auditive de transmission congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5946841000241114 surdité congénitale de transmission fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5946851000241112 perte auditive de transmission congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital conductive hearing loss Is a Conductive hearing loss true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital conductive hearing loss Is a Decreased hearing true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital conductive hearing loss Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital conductive hearing loss Interprets entité observable fonctionnelle false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital conductive hearing loss Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital conductive hearing loss Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital conductive hearing loss Finding site Ear structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital conductive hearing loss Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital conductive hearing loss Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital conductive hearing loss Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital conductive hearing loss Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital conductive hearing loss Finding site Ear structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital conductive hearing loss Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Facial dysmorphism, conductive hearing loss, heart defect syndrome Is a True Congenital conductive hearing loss Inferred relationship Existential restriction modifier (core metadata concept)
Conductive hearing loss, malformation of external ear syndrome (disorder) Is a True Congenital conductive hearing loss Inferred relationship Existential restriction modifier (core metadata concept)
Multiple epiphyseal dysplasia Beighton type (disorder) Is a True Congenital conductive hearing loss Inferred relationship Existential restriction modifier (core metadata concept)
Johnson neuroectodermal syndrome (disorder) Is a True Congenital conductive hearing loss Inferred relationship Existential restriction modifier (core metadata concept)
Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome (disorder) Is a True Congenital conductive hearing loss Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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