LOINC
Version 2.72

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

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https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=99972-2