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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

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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