| Name | Value |
|---|---|
| CODE | 99972 |
| COMPONENT | HEARING LOSS MULTIGENE ANALYSIS |
| CHECK DIGIT | 2 |
| PROPERTY | Finding |
| DATE LAST CHANGED | 2022-02-16 00:00:00 |
| CHANGE TYPE | ADD |
| TIME ASPECT | POINT |
| SYSTEM | BLD/TISS |
| SCALE TYPE | Document |
| METHOD TYPE | MOLGEN |
| CLASS | MOLPATH |
| FULLY SPECIFIED NAME | HEARING LOSS MULTIGENE ANALYSIS:FIND:PT:BLD/TISS:DOC:MOLGEN |
| SHORTNAME | HEARING LOSS MULTIGENE ANALY BLD/T |
| LONG COMMON NAME | HEARING LOSS MULTIGENE ANALYSIS IN BLOOD OR TISSUE BY MOLECULAR GENETICS METHOD |
| COMMENTS | Multigene analysis for both syndromic and non-syndromic forms of hearing loss. G enetic 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 treatm ent options for the patient.[NCBI Books: NBK1434] |
| MASTER ENTRY FOR VUID | YES |
| VUID | 5342655 |
| EFFECTIVE DATE/TIME |
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