Test Catalog

NGHHA/64939:
Hereditary Hemolytic Anemia Comprehensive Sequencing, Varies

CPT Code Information Current Value

81242-FANCC

81350-UGT1A

81364-HBB

81249-G6PD

81405 x 3-PKLR, RPS19, SLC2A1

81479-AK1, ALDOA, ANK1, C15ORF41, CD59, CDAN1, EPB41, PB42, FANCA, FANCG, GATA1, GCLC, GPI, GSS, CYPC, HBD, HK1, HMOX1, KIF23, KLF1, NT5C3A, PFKM, PIEZO1, RHAG, SEC23B, SLC4A1, SPTA1, SPTB, STOM, TPI1


CPT Code Information Value Prior to 1/01/2018 7:03am

81242-FANCC (Fanconi anemia, complementation group C) (eg, Fanconi anemia, type C) gene analysis, common variant (eg, IVS4+4A>T)

81350-UGT1A1 (UDP glucuronosyltransferase 1 family, polypeptide A1) (eg, irinotecan metabolism), gene analysis, common variants (e.g., *28, *36, *37)

81404-Molecular pathology procedure, Level 5 (eg, analysis of 2-5 exons by DNA sequence analysis, mutation scanning or duplication/deletion variants of 6-10 exons, or characterization of a dynamic mutation disorder/triplet repeat by Southern blot analysis)

81405 x 3-PKLR, RPS19, SLC2A1, 81479 AK1, ALDOA, ANK1, C15ORF41, CD59, CDAN1, EPB41, PB42, FANCA, FANCG, G6PD, GATA1, GCLC, GPI, GSS, GYPC, HBD, HK1, HMOX1, KIF23, KLF1, NT5C3A, PFKM, PGK1, PIEZO1, RHAG, SEC23B, SLC4A1, SPTA1, SPTB, STOM, TPI1

81479-Unlisted molecular pathology procedure