Code System Concept

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Code System Concept

Code System Concept Code	1260199008
Code System Concept Name	Non-syndromic genetic hearing loss (disorder)
Code System Preferred Concept Name	Non-syndromic genetic hearing loss (disorder)
Concept Status	Published
Concept Status Date	09/01/2024
Code System Name	SNOMED-CT

Concept Relationships
Concept Details

Concept Details

Code System Code	PH_SNOMED-CT
Code System OID	2.16.840.1.113883.6.96
HL7 Table 0396 Code	SCT
Superseded By Concept
SDO Concept Status	Active
SDO Concept Status Date	03/01/2024
SDO Date Created	01/31/2023
SDO Date Revised	01/31/2023
Description	Deafness is the most frequent form of sensorial deficit. In the vast majority of cases, the deafness is termed nonsyndromic or isolated and the hearing loss is the only clinical anomaly reported. The majority of cases presenting at birth concern perceptive deafness (with a neurosensory origin associated with the inner ear) rather than conductive deafness (anomalies in the amplification of sound waves between the middle ear and the outer ear).
Sequence

Extended Properties

No extended properties.

Concept Alternate Designations

SDO Designation ID	Concept Designation Description	Status	Designation Type	PHIN Preferred Term Flag	Code Flag
5159685018	Non-syndromic genetic deafness	Active	Synonym	false	false
5159686017	Non-syndromic genetic hearing loss	Active	Synonym	false	false
5159688016	Isolated genetic hearing loss	Active	Synonym	false	false
5159689012	Isolated genetic deafness	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Clinical Finding (NNDSS)	2 , 1

Parent Concepts Parent Concepts Parent/Child (Relationship Type) Decreased hearing (finding) {103276001 , SNOMED-CT } Genetic disease (disorder) {782964007 , SNOMED-CT } Hearing loss (disorder) {15188001 , SNOMED-CT }	Other Relationships No other relationships present.
Child Concepts Non-syndromic genetic hearing loss (disorder) {1260199008 , SNOMED-CT } Parent/Child (Relationship Type) Postlingual non-syndromic genetic deafness (disorder) {764097002 , SNOMED-CT } Prelingual non-syndromic genetic deafness (disorder) {764098007 , SNOMED-CT }

Page last reviewed:June 20, 2024
Page last updated:June 20, 2024
Content source:
- Centers for Disease Control and Prevention,