Genetic Test Details

CMT/HMN/HSAN Panel

Test Information

Title
CMT/HMN/HSAN Panel
Lab
Lab
Category
Neurogenetics
Sub Category
Neuromuscular Disease
Gene/Platform/Region List
AARS1, ABCA1, ABHD12, AGTPBP1, AIFM1, APTX, ARHGEF10, ARSA, ATL1, ATL3, ATM, ATP1A1, ATP7A, B4GALNT1, BAG3, BCKDHB, BICD2, BSCL2, CADM3, CCT5, CD59, CFAP276, CHCHD10, CLTCL1, CNTNAP1, COA7, COX6A1, CPOX, CTDP1, CYP27A1, DARS2, DCAF8, DCTN1, DEGS1, DGAT2, DHTKD1, DNAJB2, DNM2, DNMT1, DST, DYNC1H1, EGR2, ELP1, ERCC6, ERCC8, FAH, FBLN5, FBXO38, FGD4, FIG4, FLVCR1, FXN, GALC, GAN, GARS1, GBA2, GBF1, GDAP1, GJB1, GJB3, GJC2, GLA, GNB4, HADHA, HADHB, HARS1, HINT1, HK1, HMBS, HOXD10, HSPB1, HSPB3, HSPB8, HYCC1, IARS2, IGHMBP2, INF2, ITPR3, JAG1, KARS1, KCNA2, KIF1A, KIF1B, KIF5A, LAMP2, LDB3, LITAF, LMNA, LRSAM1, LYST, MARS1, MCM3AP, MEGF10, MFN2, MMACHC, MME, MORC2, MPV17, MPZ, MT-ATP6, MTMR2, MTRFR, MT-RNR1, MT-TL1, MTTP, NAGA, NAGLU, NARS1, NDRG1, NEFH, NEFL, NGF, NHERF1, NMNAT2, NTRK1, OPA1, OPA3, PCK2, PDHA1, PDK3, PEX10, PEX7, PHYH, PLEKHG5, PMM2, PMP2, PMP22, PNKP, POLG, POLR3A, PPOX, PRDM12, PRNP, PRPS1, PRX, PTPN11, RAB7A, REEP1, RETREG1, RFC1, SACS, SBF1, SBF2, SCN10A, SCN11A, SCN9A, SCO2, SEPTIN9, SETX, SGPL1, SH3TC2, SIGMAR1, SLC12A6, SLC25A19, SLC25A46, SLC52A2, SLC52A3, SLC5A7, SMN1, SORD, SOX10, SPAST, SPG11, SPTBN4, SPTLC1, SPTLC2, SURF1, SYT2, TFG, TRIM2, TRPA1, TRPV4, TTPA, TTR, TUBB3, TYMP, UBA1, VCP, VPS13A, VRK1, VWA1, WARS1, WNK1, XK, XPA, YARS1, ZFHX2, ZFYVE26
Test type
Gene Panel
Samples Accepted
Blood , DNA
Indications
Carrier Cascade Testing , Diagnosis
Test Methodology
Sequencing
Disease/Condition
Charcot Marie Tooth disease (CMT), hereditary motor neuropathy (HMN), hereditary sensory and autonomic neuropathy (HSAN)

Last Updated: June 23, 2025