CPT® Code Modifiers

-/+ Deleted, Replaced, Expanded Codes

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Genetic Testing Code Modifiers

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Neurologic, Non-Neoplastic

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5A  ASPA, commonly called Aspartoacylase A (Canavan disease)
5B FMR-1 (fragile X, FRAXA, syndrome)
5C FRDA, commonly called Frataxin (Freidreich ataxia)
5D HD, commonly called Huntington (Huntington’s disease)
5E GABRA5, NIPA1, UBE3A, or ANCR GABRA (Prader Willi-Angelman syndrome)
5F  GJB2, commonly called Connexin-26 (hereditary hearing loss) Connexin-32 (GJB2) (hereditary deafnes
5G GJB1, commonly called Connexin-32 (X-linked Charcot-Marie-Tooth disease)
5H SNRPN (Prader Willi-Angelman syndrome)
5I SCA1, commonly called Ataxin-1 (spinocerebellar ataxia, type 1)
5J SCA2, commonly called Ataxin-2 (spinocerebellar ataxia, type 2)
5K MJD, commonly called Ataxin-3 (spinocerebellar ataxia, type 3, Machado-Joseph disease)
5L CACNA1A (spinocerebellar ataxia, type 6)
5M ATXN7 Ataxin-7 (spinocerebellar ataxia, type 7)
5N PMP-22 (Charcot-Marie-Tooth disease, type 1A)
5O MECP2 (Rett syndrome)
5Z Neurologic, non-neoplastic, not otherwise specified
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