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764098007: Prelingual non-syndromic genetic deafness (disorder)

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3646039018 Isolated prelingual genetic deafness en Synonym Active Case insensitive SNOMED CT core
3646040016 Prelingual non-syndromic genetic deafness (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3646041017 Prelingual non-syndromic genetic deafness en Synonym Active Case insensitive SNOMED CT core
3646042012 A rare genetically highly heterogeneous otorhinolaryngologic disease, resulting from inner and/or middle ear or hearing nerve anomalies, with typical characteristics of bilateral, severe to profound hearing loss (mean sensorineural hearing impairment of 60 dB or more for 500-1,000-, and 2,000-Hz frequency tones in the better ear) which occurs before the onset of speech development and is not associated with visible external ear abnormalities or any other medical problems. It is usually nonprogressive and impedes oral language acquisition. en Definition Inactive Case sensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Prelingual non-syndromic genetic deafness Pathological process Pathological developmental process false Inferred relationship Some 1
Prelingual non-syndromic genetic deafness Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
Prelingual non-syndromic genetic deafness Is a Congenital sensorineural hearing loss false Inferred relationship Some
Prelingual non-syndromic genetic deafness Is a Genetic disease false Inferred relationship Some
Prelingual non-syndromic genetic deafness Is a Non-syndromic genetic hearing loss true Inferred relationship Some
Prelingual non-syndromic genetic deafness Finding site Structure of auditory system true Inferred relationship Some 2
Prelingual non-syndromic genetic deafness Interprets Hearing true Inferred relationship Some 1
Prelingual non-syndromic genetic deafness Has interpretation Decreased true Inferred relationship Some 1
Prelingual non-syndromic genetic deafness Is a Sensorineural hearing loss false Inferred relationship Some
Prelingual non-syndromic genetic deafness Is a Congenital anomaly of ear with impairment of hearing false Inferred relationship Some
Prelingual non-syndromic genetic deafness Is a Auditory system hereditary disorder false Inferred relationship Some
Prelingual non-syndromic genetic deafness Interprets Hearing false Inferred relationship Some 2
Prelingual non-syndromic genetic deafness Interprets Functional observable false Inferred relationship Some
Prelingual non-syndromic genetic deafness Associated morphology Developmental abnormality false Inferred relationship Some 1
Prelingual non-syndromic genetic deafness Occurrence Congenital false Inferred relationship Some 1
Prelingual non-syndromic genetic deafness Finding site Ear structure false Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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