CPT® Code Modifiers

-/+ Deleted, Replaced, Expanded Codes

section notes

Genetic Testing Code Modifiers

section notes

Neurologic, Non-Neoplastic

section notes
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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