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Afghanistan
Albania
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American Samoa
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Anguilla
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Argentina
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Cambodia
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Canada
Cape Verde
Cayman Islands
Central African Republic
Chad
Chile
China
Christmas Island
Cocos (Keeling) Islands
Colombia
Comoros
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Cook Islands
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Cote d'Ivoire
Croatia
Cuba
Curaçao
Cyprus
Czech Republic
Democratic Republic of the Congo
Denmark
Djibouti
Dominica
Dominican Republic
Ecuador
Egypt
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Equatorial Guinea
Eritrea
Estonia
Ethiopia
Falkland Islands
Faroe Islands
Fiji
Finland
France
French Polynesia
Gabon
The Gambia
Georgia
Germany
Ghana
Gibraltar
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Greenland
Grenada
Guadeloupe
Guam
Guatemala
Guernsey
Guinea
Guinea-Bissau
Guyana
Haiti
Honduras
Hong Kong
Hungary
Iceland
India
Indonesia
Iran
Iraq
Ireland
Israel
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Jamaica
Japan
Jersey
Jordan
Kazakhstan
Kenya
Kiribati
North Korea
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Kosovo
Kuwait
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Laos
Latvia
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Liberia
Libya
Liechtenstein
Lithuania
Luxembourg
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Madagascar
Malawi
Malaysia
Maldives
Mali
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Marshall Islands
Martinique
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Mauritius
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Micronesia
Moldova
Monaco
Mongolia
Montenegro
Montserrat
Morocco
Mozambique
Myanmar
Nagorno-Karabakh
Namibia
Nauru
Nepal
Netherlands
Netherlands Antilles
New Caledonia
New Zealand
Nicaragua
Niger
Nigeria
Niue
Norfolk Island
Turkish Republic of Northern Cyprus
Northern Mariana
Norway
Oman
Pakistan
Palau
Palestine
Panama
Papua New Guinea
Paraguay
Peru
Philippines
Pitcairn Islands
Poland
Portugal
Puerto Rico
Qatar
Republic of the Congo
Romania
Russia
Rwanda
Saint Barthelemy
Saint Helena
Saint Kitts and Nevis
Saint Lucia
Saint Martin
Saint Pierre and Miquelon
Saint Vincent and the Grenadines
Samoa
San Marino
Sao Tome and Principe
Saudi Arabia
Senegal
Serbia
Seychelles
Sierra Leone
Singapore
Slovakia
Slovenia
Solomon Islands
Somalia
Somaliland
South Africa
South Ossetia
South Sudan
Spain
Sri Lanka
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Svalbard
eSwatini
Sweden
Switzerland
Syria
Taiwan
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Thailand
Timor-Leste
Togo
Tokelau
Tonga
Transnistria Pridnestrovie
Trinidad and Tobago
Tristan da Cunha
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What is your CMT type?
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CMT Type 1 (CMT1)
CMT Type 2 (CMT2)
CMT Type 3 (CMT3) – Historic CMT Type
CMT4
CMTX (X-Linked CMT)
Distal Hereditary Motor Neuropathy (dHMN, aka HMN)
Distal Spinal Muscular Atrophy (dSMA)
Dominant Intermediate CMT (CMTDI)
Giant Axonal Neuropathy (GAN)
Hereditary Motor and Sensory Neuropathy (HMSN)
Hereditary Sensory and Autonomic Neuropathy (HSAN)
Hereditary Sensory Neuropathy (HSN)
Recessive Intermediate CMT (CMTRI)
Roussy–Lévy Syndrome – Historic CMT Type
Spinal Muscular Atrophy - Lower Extremity Predominant
Unclassified
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Variant of Unknown or Uncertain Significance (VUS)
CMT1A (Gene: PMP22)
CMT1B (Gene: MPZ)
CMT1C (Gene: LITAF)
CMT1D (Gene: EGR2)
CMT1E (Gene: PMP22)
CMT1F (Gene: NEFL)
CMT1G (Gene: PMP2)
CMT1H (Gene: FBLN5)
CMT1I (Gene: POLR3B)
CMT1J (Gene: ITPR3)
HNPP (Gene: PMP22)
CMT2A (aka CMT2A1, CMT2A2, CMT2A2A) (Gene: MFN2)
CMT2A2B (Gene: MFN2)
CMT2B (Gene: RAB7A)
CMT2B1 (Gene: LMNA)
CMT2B2 (Gene: PNKP)
CMT2B3 (Gene: GDAP1)
CMT2B4 (Gene: MFN2)
CMT2B5 (Gene: NEFL)
CMT2C (Gene: TRPV4)
CMT2CC (Gene: NEFH)
CMT2D (Gene: GARS1)
CMT2DD (Gene: ATP1A1)
CMT2E (Gene: NEFL)
CMT2EE (Gene: MPV17)
CMT2F (Gene: HSPB1)
CMT2FF (Gene: CADM3)
CMT2GG (aka CMTDIA) (Gene: GBF1)
CMT2HH (Gene: JAG1)
CMT2I (Gene: MPZ)
CMT2II (Gene: SLC12A6)
CMT2J (Gene: MPZ)
CMT2K (Gene: GDAP1)
CMT2L (Gene: HSPB8)
CMT2M (Gene: DNM2)
CMT2N (Gene: AARS1)
CMT2O (Gene: DYNC1H1)
CMT2P (Gene: LRSAM1)
CMT2Q (Gene: DHTKD1)
CMT2R (Gene: TRIM2)
CMT2S (Gene: IGHMBP2)
CMT2T (Gene: MME)
CMT2U (Gene: MARS1)
CMT2V (Gene: NAGLU)
CMT2W (Gene: HARS1)
CMT2X (Gene: SPG11)
CMT2Y (Gene: VCP)
CMT2Z (Gene: MORC2)
CMT3
CMT4A (Gene: GDAP1)
CMT4B1 (Gene: MTMR2)
CMT4B2 (Gene: SBF2)
CMT4B3 (Gene: SBF1)
CMT4C (Gene: SH3TC2)
CMT4D (Gene: NDRG1)
CMT4E (Gene: EGR2)
CMT4F (Gene: PRX)
CMT4G (aka HMSN-Russe Type (HMSNR)) (Gene: HK1)
CMT4H (Gene: FGD4)
CMT4J (Gene: FIG4)
CMT4K (Gene: SURF1)
CMTX1 (aka CMT1X, CMTX) (Gene: GJB1)
CMTX2 (Gene: Unknown - Xp22.2)
CMTX3 (Gene: Transgenic 8q24.3 and Xq27.1)
CMTX4 (Gene: AIFM1)
CMTX5 (Gene: PRPS1)
CMTX6 (Gene: PDK3)
CMTDIA (aka CMT2GG) (Gene: GBF1)
CMTDIB (Gene: DNM2)
CMTDIC (Gene: YARS1)
CMTDID (Gene: MPZ)
CMTDIE (Gene: INF2)
CMTDIF (Gene: GNB4)
CMTDIG (Gene: NEFL)
CMTRIA (Gene: GDAP1)
CMTRIB (Gene: KARS1)
CMTRIC (Gene: PLEKHG5)
CMTRID (Gene: COX6A1)
CMTRIE (Gene: KCTD11)
dHMN-AARS1 (Gene: AARS1)
dHMN-COQ7 (Gene: COQ7)
dHMN-1 (Gene: Unknown - 7q34-q36)
dHMN-2A (Gene: HSPB8)
dHMN-2B (Gene: HSPB1)
dHMN-2C (Gene: HSPB3)
dHMN-2D (Gene: FBXO38)
dHMN-5A (Gene: GARS1)
dHMN-5B (Gene: REEP1)
dHMN-5C (Gene: BSCL2)
dHMN-6 (aka dSMA-1)(Gene: IGHMBP2)
dHMN-7A (Gene: SLC5A7)
dHMN-7B (Gene: DCTN1)
dHMN-8 (Gene: TRPV4)
dHMN-9 (Gene: WARS1)
dHMN-MYH14 (Gene: MYH14)
dHMN2-SIGMAR1 (Gene: SIGMAR1)
dHMN1-UBE3C (Gene: UBE3C)
dHMN-VWA1 (Gene: VWA1)
dSMA (Gene: VRK1)
dSMA-4 (Gene: PLEKHG5)
dSMA-5 (Gene: DNAJB2)
dSMAX-2 (Gene: UBA1)
dSMAX-3 (Gene: ATP7A)
GAN-1 (Gene: GAN)
GAN-2 (Gene: DCAF8)
HMSN-4 (aka Refsum Disease) (Gene: PHYH)
HMSN-5 (Gene: Unknown - 4q34.3-q35.2)
HMSN-6A (Gene: MFN2)
HMSN-6B (Gene: SLC25A46)
HMSN-6C (Gene: PDXK)
HMSN-Okinawa Type (Gene: TFG)
HSAN-1A (Gene: SPTLC1)
HSAN-1B (Gene: Unknown but Mapped to 3p22-p24)
HSAN-1C (Gene: SPTLC2)
HSAN-2A (Gene: WNK1)
HSAN-2B (Gene: RETREG1)
HSAN-2D (Gene: SCN9A)
HSAN-3 (Gene: ELP1)
HSAN-4 (Gene: NTRK1)
HSAN-5 (Gene: NGF)
HSAN-6 (Gene: DST)
HSAN-7 (Gene: SCN11A)
HSAN-8 (Gene: PRDM12)
HSAN-9 (Gene: TECPR2)
HSN-FLVCR1 (Gene: FLVCR1)
HSN w/SPG (Gene: CCT5)
HSN-1A (Gene: SPTLC1)
HSN-1B (Gene: Unknown - 3p22-p24)
HSN-1C (Gene: SPTLC2)
HSN-1D (Gene: ATL1)
HSN-1E (Gene: DNMT1)
HSN-1F (Gene: ATL3)
HSN-2A (Gene: WNK1)
HSN-2C (Gene: KIF1A)
Roussy–Lévy Syndrome
SMA-LEP-1 (Gene: DYNC1H1)
SMA-LEP-2A (Gene: BICD2)
SMA-LEP-2B (Gene: BICD2)
CMT-ABHD12 (Gene: ABHD12)
CMT-ARHGEF10 (Gene: ARHGEF10)
CMT-ATP6 (Gene: ATP6)
CMT-BAG3 (Gene: BAG3)
CMT-C19ORF12 (Gene: C19ORF12)
CMT-CFAP276 (Gene: CFAP276)
CMT-CHCHD10 (Gene: CHCHD10)
CMT-CNTNAP1 (Gene: CNTNAP1)
CMT-COA7 (Gene: COA7)
CMT-CRYAB (Gene: CRYAB)
CTDP1-CMT (Gene: CTDP1)
CMT-DGAT2 (Gene: DGAT2)
CMT-DHX9 (Gene: DHX9)
CMT-DRP2 (Gene: DRP2)
CMT-DST (Gene: DST)
CMT-HADHB (Gene: HADHB)
CMT-HINT1 (Gene: HINT1)
CMT-INSC (Gene: INSC)
CMT-KIF5A (Gene: KIF5A)
CMT-MCM3AP (Gene: MCM3AP)
CMT-MTRFR (Gene: MTRFR)
CMT-NOTCH2NLC (Gene: NOTCH2NLC)
CMT-MYO9B (Gene: MYO9B)
CMT-NARS1 (Gene: NARS1)
CMT-NDUFS6 (Gene: NDUFS6)
CMT-POLG (Gene: POLG)
CMT-PSAT1 (Gene: PSAT1)
CMT-RFC1 (aka CANVAS) (Gene: RFC1)
CMT-SACS (Gene: SACS)
CMT-SARS1 (Gene: SARS1)
CMT-SEPT9 (Gene: SEPT9)
CMT-SCO2 (Gene: SCO2)
CMT-SCYL1 (Gene: SCYL1)
CMT-SETX (Gene: SETX)
CMT-SGPL1 (Gene: SGPL1)
CMT-SORD (aka SORD-Deficiency, Sorbitol Dehydrogenase-Deficiency) (Gene: SORD)
CMT-SYT2 (Gene: SYT2)
CMT-TUBB3 (Gene: TUBB3)
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