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Disease	Synonyms	Description	Articles
Charcot-Marie-Tooth disease axonal type 2X	autosomal recessive axonal Charcot-Marie-Tooth dis.. [+] autosomal recessive axonal Charcot-Marie-Tooth disease type 2X; Charcot-Marie-Tooth neuropathy type 2X; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the SPG11 gene on chromosome 15q21. [-]
Charcot-Marie-Tooth disease axonal type 2Z	autosomal dominant axonal Charcot-Marie-Tooth dise.. [+] autosomal dominant axonal Charcot-Marie-Tooth disease type 2Z; Charcot-Marie-Tooth neuropathy type 2Z; CMT2Z; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the MORC2 gene on chromosome 22q12. [-]
Charcot-Marie-Tooth disease dominant intermediate A	autosomal dominant intermediate Charcot-Marie-Toot.. [+] autosomal dominant intermediate Charcot-Marie-Tooth disease type A; Charcot-Marie-Tooth neuropathy dominant intermediate A; DI-CMTA; CMTDIA; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in variation in the region 10q24.1-q25.1. [-]
Charcot-Marie-Tooth disease dominant intermediate B	Charcot-Marie-Tooth neuropathy dominant intermedia.. [+] Charcot-Marie-Tooth neuropathy dominant intermediate B; CMTDIB; DI-CMTB; CMTDI1; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in mutation in the gene encoding dynamin-2 (DNM2). [-]
Charcot-Marie-Tooth disease dominant intermediate C	autosomal dominant intermediate Charcot-Marie-Toot.. [+] autosomal dominant intermediate Charcot-Marie-Tooth disease type C; CMTDIC; DI-CMTC; Charcot-Marie-Tooth neuropathy dominant intermediate C; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the YARS gene on chromosome 1p35. [-]
Charcot-Marie-Tooth disease dominant intermediate D	autosomal dominant intermediate Charcot-Marie-Toot.. [+] autosomal dominant intermediate Charcot-Marie-Tooth disease type D; Charcot-Marie-Tooth neuropathy dominant intermediate D; CMTDID; DI-CMTD; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23. [-]
Charcot-Marie-Tooth disease dominant intermediate E	autosomal dominant intermediate Charcot-Marie-Toot.. [+] autosomal dominant intermediate Charcot-Marie-Tooth disease type E; Charcot-Marie-Tooth disease-nephropathy syndrome; CMTDIE; Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the INF2 gene on chromosome 14q32. [-]
Charcot-Marie-Tooth disease dominant intermediate F	autosomal dominant intermediate Charcot-Marie-Toot.. [+] autosomal dominant intermediate Charcot-Marie-Tooth disease type F; CMTDIF; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the GNB4 gene on chromosome 3q28. [-]
Charcot-Marie-Tooth disease dominant intermediate G		A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the NEFL gene on chromosome 8p21. [-]
Charcot-Marie-Tooth disease intermediate type	Charcot-Marie-Tooth disease recessive intermediate.. [+] Charcot-Marie-Tooth disease recessive intermediate; Charcot-Marie-Tooth disease dominant intermediate; [-]	A Charcot-Marie-Tooth disease characterized by mot..[+] A Charcot-Marie-Tooth disease characterized by motor conduction velocities above and below 38 m/s. [-]
Charcot-Marie-Tooth disease recessive intermediate A	Charcot-Marie-Tooth neuropathy recessive intermedi.. [+] Charcot-Marie-Tooth neuropathy recessive intermediate A; CMTRIA; autosomal recessive intermediate Charcot-Marie-Tooth disease type A; RI-CMTA; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in homozygous mutation in the GDAP1 gene on chromosome 8q21. [-]
Charcot-Marie-Tooth disease recessive intermediate B	autosomal recessive intermediate Charcot-Marie-Too.. [+] autosomal recessive intermediate Charcot-Marie-Tooth disease type B; CMTRIB; RI-CMTB; Charcot-Marie-Tooth neuropathy recessive intermediate B; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in compound heterozygous mutation in the KARS gene on chromosome 16q23. [-]
Charcot-Marie-Tooth disease recessive intermediate C	CMTRIC; RI-CMT type C; RI-CMTC; autosomal recessiv.. [+] CMTRIC; RI-CMT type C; RI-CMTC; autosomal recessive intermediate Charcot-Marie-Tooth disease type C; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in homozygous or compound heterozygous mutation in the PLEKHG5 gene on chromosome 1p36. [-]
Charcot-Marie-Tooth disease recessive intermediate D	autosomal recessive intermediate Charcot-Marie-Too.. [+] autosomal recessive intermediate Charcot-Marie-Tooth disease type D; RI-CMT type D; CMTRID; [-]	A Charcot-Marie-Tooth disease intermediate type th..[+] A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in homozygous mutation in the COX6A1 gene on chromosome 12q24. [-]
Charcot-Marie-Tooth disease type 1	hereditary motor and sensory neuropathy type 1;	A Charcot-Marie-Tooth disease characterized by dem..[+] A Charcot-Marie-Tooth disease characterized by demyelination of the peripheral nerve axons. [-]	1 articles
Charcot-Marie-Tooth disease type 1A	autosomal dominant Charcot-Marie-Tooth disease wit.. [+] autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A; CMT1A; hereditary motor and sensory neuropathy 1A; HMSN1A; Charcot-Marie-Tooth neuropathy type 1A; microduplication 17p12; [-]	A Charcot-Marie-Tooth disease type 1 that has_mate..[+] A Charcot-Marie-Tooth disease type 1 that has_material_basis_in duplication of, or mutation in, the gene encoding peripheral myelin protein-22 (PMP22). [-]
Charcot-Marie-Tooth disease type 1B	autosomal dominant Charcot-Marie-Tooth disease wit.. [+] autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B ; Charcot-Marie-Tooth neuropathy type 1B; CMT1B; hereditary motor and sensory neuropathy IB; HMSN IB; HMSN1B; peroneal muscular atrophy; Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy; [-]	A Charcot-Marie-Tooth disease type 1 that has_mate..[+] A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the gene encoding myelin protein zero (MPZ). [-]	1 articles
Charcot-Marie-Tooth disease type 1C	Charcot-Marie-Tooth neuropathy type 1C; CMT1C; HMS.. [+] Charcot-Marie-Tooth neuropathy type 1C; CMT1C; HMSN IC; HMSN1C; neuropathy hereditary motor and sensory type 1C; CMT slow nerve conduction type C; [-]	A Charcot-Marie-Tooth disease type 1 that has_mate..[+] A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13. [-]
Charcot-Marie-Tooth disease type 1D	Charcot-Marie-Tooth neuropathy type 1D; CMT1D; HMS.. [+] Charcot-Marie-Tooth neuropathy type 1D; CMT1D; HMSN ID; HMSN1D; hereditary motor and sensory neuropathy 1D; [-]	A Charcot-Marie-Tooth disease type 1 that has_mate..[+] A Charcot-Marie-Tooth disease type 1 that has_material_basis_in mutation in the early growth response gene-2 (EGR2). [-]
Charcot-Marie-Tooth disease type 1E	autosomal dominant Charcot-Marie-Tooth neuropathy .. [+] autosomal dominant Charcot-Marie-Tooth neuropathy and deafness; Charcot-Marie-Tooth disease and deafness; Charcot-Marie-Tooth disease demyelinating type 1E; Charcot-Marie-Tooth disease-deafness; CMT1E; [-]	A Charcot-Marie-Tooth disease type 1 that has_mate..[+] A Charcot-Marie-Tooth disease type 1 that has_material_basis_in autosomal dominant mutation in the peripheral myelin protein-22 gene (PMP22). [-]
Charcot-Marie-Tooth disease type 1F	Charcot-Marie-Tooth neuropathy type 1F; CMT1F;	A Charcot-Marie-Tooth disease type 1 that has_mate..[+] A Charcot-Marie-Tooth disease type 1 that has_material_basis_in mutation in the NEFL gene. [-]
Charcot-Marie-Tooth disease type 1G	CMT1G; PMP2-related Charcot-Marie-Tooth disease ty.. [+] CMT1G; PMP2-related Charcot-Marie-Tooth disease type 1; PMP2-related Charcot-Marie-Tooth neuropathy type 1; PMP2-related hereditary motor and sensory neuropathy type 1; PMP2-related CMT1; [-]	A Charcot-Marie-Tooth disease type 1 characterized..[+] A Charcot-Marie-Tooth disease type 1 characterized by distal muscle weakness and atrophy with onset in the first or second decade of life that has_material_basis_in heterozygous mutation in the PMP2 gene on chromosome 8q21.13. [-]
Charcot-Marie-Tooth disease type 2	hereditary motor and sensory neuropathy Guadalajar.. [+] hereditary motor and sensory neuropathy Guadalajara neuronal type; hereditary motor and sensory neuropathy type 2; hereditary motor and sensory neuropathy Okinawa type; [-]	A Charcot-Marie-Tooth disease characterized by abn..[+] A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell. [-]	1 articles
Charcot-Marie-Tooth disease type 2A1	autosomal dominant Charcot-Marie-Tooth disease axo.. [+] autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1; Charcot-Marie-Tooth disease neuronal type 2A1; CMT2A1; hereditary motor and sensory neuropathy IIA1; HMSN IIA1; HMSN2A1; Charcot-Marie-Tooth neuropathy type 2A1; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the KIF1B gene on chromosome 1p36. [-]
Charcot-Marie-Tooth disease type 2A2A	autosomal dominant axonal Charcot-Marie-Tooth dise.. [+] autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2; Charcot-Marie-Tooth neuropathy type 2A2; CMT2A2; hereditary motor and sensory neuropathy IIA2; HMSN IIA2; HMSN2A2; Charcot-Marie-Tooth neuronal type 2A2; CMT2A2A; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the MFN2 gene on chromosome 1p36.22. [-]
Charcot-Marie-Tooth disease type 2A2B	AR-CMT2, Ouvrier type; Charcot-Marie-Tooth disease.. [+] AR-CMT2, Ouvrier type; Charcot-Marie-Tooth disease, axonal, type 2A2B; CMT2A2B; SEOAN due to MFN2 deficiency; severe early-onset axonal neuropathy due to MFN2 deficiency; autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type; [-]	A Charcot-Marie-Tooth disease type 2 characterized..[+] A Charcot-Marie-Tooth disease type 2 characterized by onset of peripheral neuropathy in the first years of life that has_material_basis_in homozygous or compound heterozygous mutation in the MFN2 gene on chromosome 1p36.22. [-]
Charcot-Marie-Tooth disease type 2B	Charcot-Marie-Tooth neuropathy type 2B; CMT2B; HMS.. [+] Charcot-Marie-Tooth neuropathy type 2B; CMT2B; HMSN IIB; HMSN2B; autosomal dominant Charcot-Marie-Tooth disease type 2B; hereditary motor and sensory nueropathy IIB; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the RAB7 gene on chromosome 3q21. [-]	1 articles
Charcot-Marie-Tooth disease type 2B1	autosomal recessive axonal Charcot-Marie-Tooth dis.. [+] autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1; autosomal recessive axonal CMT4C1; Charcot-Marie-Tooth disease neuronal type 2B1; Charcot-Marie-Tooth neuropathy type 2B1; CMT2B1; autosomal recessive Charcot-Marie-Tooth disease type 2B1; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous mutation in the lamin A/C gene (LMNA) on chromosome 1q22. [-]
Charcot-Marie-Tooth disease type 2B2	ARCMT2B; autosomal recessive axonal Charcot-Marie-.. [+] ARCMT2B; autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2; Autosomal recessive axonal CMT4C3; Charcot-Marie-Tooth disease neuronal type 2B2; Charcot-Marie-Tooth neuropathy type 2B2; CMT2B2; AR-CMT2B2; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous mutation in the MED25 gene. [-]
Charcot-Marie-Tooth disease type 2D	autosomal dominant Charcot-Marie-Tooth disease typ.. [+] autosomal dominant Charcot-Marie-Tooth disease type 2D; Charcot-Marie-Tooth disease neuronal type 2D; CMT2D; Charcot-Marie-Tooth neuropathy type 2D; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in mutation in the GARS1 gene. [-]
Charcot-Marie-Tooth disease type 2DD	ATP1A1-related autosomal dominant Charcot-Marie-To.. [+] ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2; ATP1A1-related CMT2; Charcot-Marie-Tooth disease, axonal, type 2DD; Charcot-Marie-Tooth neuropathy, type 2DD; CMT2DD; [-]	A Charcot-Marie-Tooth disease type 2 characterized..[+] A Charcot-Marie-Tooth disease type 2 characterized by neuropathy mainly affecting the lower limbs that has_material_basis_in heterozygous mutation in the ATP1A1 gene on chromosome 1p13.1. [-]
Charcot-Marie-Tooth disease type 2E	autosomal dominant Charcot-Marie-Tooth disease typ.. [+] autosomal dominant Charcot-Marie-Tooth disease type 2E; CMT2E; Charcot-Marie-Tooth neuropathy type 2E; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the light polypeptide neurofilament protein gene (NEFL) on chromosome 8p21. [-]
Charcot-Marie-Tooth disease type 2EE	Charcot-Marie-Tooth disease, axonal, type 2EE; CMT.. [+] Charcot-Marie-Tooth disease, axonal, type 2EE; CMT2EE; [-]	A Charcot-Marie-Tooth disease type 2 characterized..[+] A Charcot-Marie-Tooth disease type 2 characterized by slowly progressive axonal neuropathy primarily affecting the lower limbs with onset in the first or second decades of life that has_material_basis_in homozygous or compound heterozygous mutation in the MPV17 gene on chromosome 2p23.3. [-]
Charcot-Marie-Tooth disease type 2I	Charcot-Marie-Tooth neuropathy type 2I; CMT2I;	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23. [-]
Charcot-Marie-Tooth disease type 2J	Charcot-Marie-Tooth disease type 2 with hearing lo.. [+] Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities; Charcot-Marie-Tooth neuropathy type 2J; CMT2J; [-]	A Charcot-Marie-Tooth disease type 2 characterized..[+] A Charcot-Marie-Tooth disease type 2 characterized by hearing loss and pupillary abnormalities and has_material_basis_in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23. [-]
Charcot-Marie-Tooth disease type 2R	Charcot-Marie-Tooth neuropathy type 2R; CMT2R; aut.. [+] Charcot-Marie-Tooth neuropathy type 2R; CMT2R; autosomal recessive axonal Charcot-Marie-Tooth disease type 2R; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the TRIM2 gene on chromosome 4q. [-]
Charcot-Marie-Tooth disease type 2Y	autosomal dominant axonal Charcot-Marie-Tooth type.. [+] autosomal dominant axonal Charcot-Marie-Tooth type 2Y; autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation; CMT2 due to VCP mutation; CMT2Y; Charcot-Marie-Tooth neuropathy type 2Y; [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the VCP gene on chromosome 9p13. [-]
Charcot-Marie-Tooth disease type 3	DEJERINE-SOTTAS SYNDROME; DEJERINE-SOTTAS NEUROPAT.. [+] DEJERINE-SOTTAS SYNDROME; DEJERINE-SOTTAS NEUROPATHY; [-]	n_a
Charcot-Marie-Tooth disease type 4	hereditary motor and sensory neuropathy;	A Charcot-Marie-Tooth disease characterized by dem..[+] A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance. [-]
Charcot-Marie-Tooth disease type 4A	Charcot-Marie-Tooth neuropathy type 4A; CMT4A; aut.. [+] Charcot-Marie-Tooth neuropathy type 4A; CMT4A; autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A; [-]	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the gene encoding ganglioside-induced differentiation-associated protein-1 (GDAP1) on chromosome 8q21. [-]
Charcot-Marie-Tooth disease type 4B1	autosomal recessive Charcot-Marie-Tooth disease wi.. [+] autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1; Charcot-Marie-Tooth neuropathy type 4B1; CMT4B1; [-]	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the gene encoding the myotubularin-related protein-2 (MTMR2). [-]
Charcot-Marie-Tooth disease type 4B2	autosomal recessive Charcot-Marie-Tooth disease wi.. [+] autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B2; CMT4B2; Charcot-Marie-Tooth neuropathy type 4B2; [-]	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the SBF2 gene. [-]
Charcot-Marie-Tooth disease type 4B3	CMT4B3;	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the SBF1 gene on chromosome 22q. [-]
Charcot-Marie-Tooth disease type 4C	autosomal recessive demyelinating Charcot-Marie-To.. [+] autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4C; CMT4C; Charcot-Marie-Tooth neuropathy type 4C; [-]	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the SH3TC2 gene. [-]
Charcot-Marie-Tooth disease type 4D	hereditary motor and sensory neuropathy LOM type; .. [+] hereditary motor and sensory neuropathy LOM type; HMSN-Lom; HMSN4D; autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D; CMT4D; hereditary motor abd sensory neuropathy LOM type; HMSN Lom type; HMSNL; Charcot-Marie-Tooth neuropathy type 4D; [-]	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the N-myc downstream-regulated gene-1 (NDRG1) on chromosome 8q24. [-]
Charcot-Marie-Tooth disease type 4E	autosomal recessive congenital hypomyelinating or .. [+] autosomal recessive congenital hypomyelinating or amyelinating neuropathy; Charcot-Marie-Tooth neuropathy type 4E; Neuropathy, congenital hypomyelinating, 1; CMT4E; [-]	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or heterozygous mutation in the EGR2 gene on chromosome 10q21 or by heterozygous mutation in the MPZ gene on chromosome 1q23. [-]
Charcot-Marie-Tooth disease type 4F	CMT4F;	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the periaxin gene (PRX) on chromosome 19q13. [-]
Charcot-Marie-Tooth disease type 4G	autosomal recessive Charcot-Marie-Tooth disease ty.. [+] autosomal recessive Charcot-Marie-Tooth disease type 4G; CMT4G; hereditary motor and sensory neuropathy Russe type; HMSNR; Charcot-Marie-Tooth neuropathy type 4G; [-]	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22. [-]
Charcot-Marie-Tooth disease type 4H	autosomal recessive demyelinating Charcot-Marie-To.. [+] autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4H; Charcot-Marie-Tooth neuropathy type 4H; CMT4H; autosomal recessive Charcot-Marie-Tooth disease type 4H; [-]	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutations in the gene encoding frabin (FGD4). [-]
Charcot-Marie-Tooth disease type 4J	autosomal recessive Charcot-Marie-Tooth disease ty.. [+] autosomal recessive Charcot-Marie-Tooth disease type 4J; CMT4J; [-]	A Charcot-Marie-Tooth disease type 4 that has_mate..[+] A Charcot-Marie-Tooth disease type 4 that has_material_basis_in compound heterozygous mutations in the FIG4 gene on chromosome 6q21. [-]

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