99972-2Hearing loss multigene analysis in Blood or Tissue by Molecular genetics methodActive
Term Description
Multigene analysis for both syndromic and non-syndromic forms of hearing loss. Genetic forms of hearing loss may be classified as autosomal dominant, recessive, X-linked or mitochondrial. Determining the cause of hearing loss, whether it is acquired or genetic, is useful for diagnosis, prognosis, and determining treatment options for the patient.[NCBI Books:NBK1434]
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Hearing loss multigene analysis
- Property
- Find
- Time
- Pt
- System
- Bld/Tiss
- Scale
- Doc
- Method
- Molgen
Additional Names
- Short Name
- Hearing loss multigene analy Bld/T
- Display Name
- Hearing loss multigene analysis Molgen Doc (Bld/Tiss)
- Consumer Name Alpha
- Hearing loss multigene analysis, Blood or tissue specimen
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.72
- Last Updated
- Version 2.72
- Order vs. Observation
- Both
LOINC FHIR® API Example - CodeSystem Request Get Info
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=99972-2
LOINC Copyright
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