Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
Code System Concept Code | 95828007 |
Code System Concept Name | Congenital deafness (disorder) |
Code System Preferred Concept Name | Congenital deafness (disorder) |
Concept Status | Published |
Concept Status Date | 09/01/2024 |
Code System Name | SNOMED-CT |
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Superseded By Concept | |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 | 07/31/2019 |
SDO Date Created | 01/31/2002 |
SDO Date Revised | 07/31/2019 |
Description | |
Sequence |
Extended Properties
No extended properties.
Concept Alternate Designations
SDO Designation ID | Concept Designation Description | Status | Designation Type | PHIN Preferred Term Flag | Code Flag |
---|---|---|---|---|---|
158711011 | Congenital deafness | Active | Synonym | false | false |
512317011 | Congenital sensorineural deafness | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
|
Other Relationships
No other relationships present.
|
Child Concepts
Congenital deafness (disorder) {95828007 , SNOMED-CT }
Parent/Child (Relationship Type)
Autosomal dominant aplasia and myelodysplasia (disorder)
{778006008
, SNOMED-CT
}
Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome (disorder)
{1332382002
, SNOMED-CT
}
Congenital deafness with labyrinthine aplasia, microtia and microdontia (disorder)
{702360007
, SNOMED-CT
}
Congenital prelingual deafness (disorder)
{699238006
, SNOMED-CT
}
Deafness, vitiligo, achalasia syndrome (disorder)
{733069009
, SNOMED-CT
}
Neutropenia, monocytopenia, deafness syndrome (disorder)
{725137007
, SNOMED-CT
}
Sinoatrial node dysfunction and deafness (disorder)
{770784003
, SNOMED-CT
}
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: