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232333009: Hearing loss associated with syndrome (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
348083015 Hearing loss associated with syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
348084014 Syndromal deafness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620384018 Hearing loss associated with syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
348083015 Hearing loss associated with syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
348083015 Hearing loss associated with syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
348084014 Syndromal deafness en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
348084014 Syndromal deafness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620384018 Hearing loss associated with syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
620384018 Hearing loss associated with syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3430851001000112 Schwerhörigkeit, syndromale, genetisch bedingte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252071000241114 perte d'audition associée à un syndrome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252081000241111 surdité syndromique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252091000241113 perte auditive associée à un syndrome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252071000241114 perte d'audition associée à un syndrome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252081000241111 surdité syndromique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6252091000241113 perte auditive associée à un syndrome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3430851001000112 Schwerhörigkeit, syndromale, genetisch bedingte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

111 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hearing loss associated with syndrome Is a Disorder of ear false Inferred relationship Existential restriction modifier (core metadata concept)
Hearing loss associated with syndrome Finding site Ear structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hearing loss associated with syndrome Finding site Structure of auditory system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hearing loss associated with syndrome Is a Hearing loss true Inferred relationship Existential restriction modifier (core metadata concept)
Hearing loss associated with syndrome Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Duane retraction syndrome with congenital deafness Is a True Hearing loss associated with syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder) Is a True Hearing loss associated with syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Keratitis ichthyosis and deafness syndrome Is a True Hearing loss associated with syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) Is a True Hearing loss associated with syndrome Inferred relationship Existential restriction modifier (core metadata concept)
A rare primary bone dysplasia characterised by microcephaly, developmental delay and intellectual disability, sensorineural hearing loss, retinal degeneration, and skeletal dysplasia. Musculoskeletal abnormalities include delayed ossification of epiphyses, spondyloepimetaphyseal dysplasia, short stature, severe spinal deformities, and severe joint laxity resulting in multiple joint dislocations. Is a True Hearing loss associated with syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Adult-onset progressive leukoencephalopathy, early-onset deafness (disorder) Is a True Hearing loss associated with syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Mitchell syndrome Is a True Hearing loss associated with syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome (disorder) Is a True Hearing loss associated with syndrome Inferred relationship Existential restriction modifier (core metadata concept)

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