Xenbase

Search Diseases

Alphabetic Search:

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

???pagination.result.count???

???pagination.result.page??? ???pagination.result.prev??? 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 ???pagination.result.next???

Disease	Synonyms	Description	Articles
Charcot-Marie-Tooth disease type 2I	CMT2I; Charcot-Marie-Tooth neuropathy type 2I	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 2B	Charcot-Marie-Tooth neuropathy type 2B; CMT2B; HMS.. [+] CMT2B; Charcot-Marie-Tooth neuropathy type 2B; 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 axonal type 2T	Charcot-Marie-Tooth neuropathy type 2T; CMT2T; AR-.. [+] CMT2T; Charcot-Marie-Tooth neuropathy type 2T; AR-CMT2T; autosomal recessive axonal Charcot-Marie-Tooth disease type 2T [-]	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 MME gene on chromosome 3q25. [-]
Charcot-Marie-Tooth disease type 2R	Charcot-Marie-Tooth neuropathy type 2R; CMT2R; aut.. [+] CMT2R; Charcot-Marie-Tooth neuropathy type 2R; 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, axonal type 2W	CMT2W; Charcot-Marie-Tooth neuropathy type 2W; aut.. [+] Charcot-Marie-Tooth neuropathy type 2W; CMT2W; autosomal dominant axonal Charcot-Marie-Tooth disease type 2W [-]	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 HARS gene on chromosome 5q31. [-]
Charcot-Marie-Tooth disease axonal type 2F	CMT2F; Charcot-Marie-Tooth neuronal type 2F; Charc.. [+] Charcot-Marie-Tooth neuronal type 2F; CMT2F; Charcot-Marie-Tooth neuropathy type 2F; autosomal dominant Charcot-Marie-Tooth disease type 2F [-]	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 gene encoding heat-shock 27-kD protein-1 (HSPB1). [-]
Charcot-Marie-Tooth disease type 2D	CMT2D; Charcot-Marie-Tooth neuropathy type 2D; Cha.. [+] Charcot-Marie-Tooth neuropathy type 2D; CMT2D; Charcot-Marie-Tooth disease neuronal type 2D; autosomal dominant Charcot-Marie-Tooth disease 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 2E	CMT2E; Charcot-Marie-Tooth neuropathy type 2E; aut.. [+] Charcot-Marie-Tooth neuropathy type 2E; CMT2E; autosomal dominant Charcot-Marie-Tooth disease 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 axonal type 2H	Charcot-Marie-Tooth disease type 2H; CMT2H; AR-CMT.. [+] CMT2H; Charcot-Marie-Tooth disease type 2H; AR-CMT2C; autosomal recessive axonal Charcot-Marie-Tooth disease with pyramidal features; autosomal recessive axonal Charcot-Marie-Tooth neuropathy with pyramidal features; Axonal Charcot-Marie-Tooth disease with pyramidal involvement; Autosomal recessive axonal CMT4C2 [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in variation in the region 8q13-q23. [-]
Charcot-Marie-Tooth disease axonal type 2K	Charcot-Marie-Tooth neuropathy axonal type 2K; ARC.. [+] Charcot-Marie-Tooth neuropathy axonal type 2K; ARCMT2K; autosomal recessive axonal Charcot-Marie-Tooth disease type 2K; autosomal recessive axonal CMT4C4; autosomal recessive Charcot-Marie-Tooth disease with hoarseness; autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K [-]	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 GDAP1 gene on chromosome 8q. [-]
Charcot-Marie-Tooth disease type 2Y	CMT2Y; Charcot-Marie-Tooth neuropathy type 2Y; CMT.. [+] Charcot-Marie-Tooth neuropathy type 2Y; CMT2Y; CMT2 due to VCP mutation; autosomal dominant axonal Charcot-Marie-Tooth type 2Y; autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation [-]	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 axonal type 2P	Charcot-Marie-Tooth neuropathy type 2P; CMT2P; Cha.. [+] CMT2P; Charcot-Marie-Tooth neuropathy type 2P; Charcot-Marie-Tooth disease type 2P [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or heterozygous mutation in the LRSAM1 gene on chromosome 9q33. [-]
Charcot-Marie-Tooth disease axonal type 2Q	Charcot-Marie-Tooth neuropathy type 2Q; CMT2Q; aut.. [+] CMT2Q; Charcot-Marie-Tooth neuropathy type 2Q; autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q; autosomal dominant Charcot-Marie-Tooth disease type 2Q [-]	A Charcot-Marie-Tooth disease type 2 that has_mate..[+] A Charcot-Marie-Tooth disease type 2 that has_material_basis_in a heterozygous loss-of-function mutation in the DHTKD1 gene on chromosome 10p14. [-]
Charcot-Marie-Tooth disease axonal type 2S	CMT2S; Charcot-Marie-Tooth disease type 2S; Charco.. [+] Charcot-Marie-Tooth disease type 2S; CMT2S; Charcot-Marie-Tooth neuropathy type 2S; autosomal recessive axonal Charcot-Marie-Tooth type 2S [-]	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 IGHMBP2 gene on chromosome 11q13. [-]
Charcot-Marie-Tooth disease axonal type 2U	CMT2U; Charcot-Marie-Tooth neuropathy type 2U; aut.. [+] Charcot-Marie-Tooth neuropathy type 2U; CMT2U; autosomal dominant axonal Charcot-Marie-Tooth disease type 2U; autosomal dominant Charcot-Marie-Tooth disease type 2U [-]	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 MARS gene on chromosome 12q13. [-]
Charcot-Marie-Tooth disease axonal type 2L	Charcot-Marie-Tooth neuropathy axonal type 2L; CMT.. [+] Charcot-Marie-Tooth neuropathy axonal type 2L; CMT2L; autosomal dominant axonal Charcot-Marie-Tooth disease type 2L; autosomal dominant Charcot-Marie-Tooth disease type 2L [-]	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 HSPB8 gene. [-]
Charcot-Marie-Tooth disease axonal type 2O	Charcot-Marie-Tooth neuropathy axonal type 2O; aut.. [+] Charcot-Marie-Tooth neuropathy axonal type 2O; autosomal dominant axonal Charcot-Marie-Tooth disease type 2O; autosomal dominant Charcot-Marie-Tooth disease type 2O [-]	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 DYNC1H1 gene on chromosome 14q32. [-]
Charcot-Marie-Tooth disease axonal type 2X	Charcot-Marie-Tooth neuropathy type 2X; autosomal .. [+] Charcot-Marie-Tooth neuropathy type 2X; autosomal recessive axonal Charcot-Marie-Tooth disease 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 2N	CMT2N; Charcot-Marie-Tooth neuropathy axonal type .. [+] CMT2N; Charcot-Marie-Tooth neuropathy axonal type 2N; autosomal dominant axonal Charcot-Marie-Tooth disease type 2N; autosomal dominant Charcot-Marie-Tooth disease type 2N [-]	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 AARS gene on chromosome 16q21. [-]
Charcot-Marie-Tooth disease axonal type 2V	Charcot-Marie-Tooth neuropathy type 2V; CMT2V; aut.. [+] CMT2V; Charcot-Marie-Tooth neuropathy type 2V; autosomal dominant Charcot-Marie-Tooth disease type 2V; autosomal dominant axonal Charcot-Marie-Tooth disease type 2V [-]	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 NAGLU gene on chromosome 17q21. [-]
Charcot-Marie-Tooth disease type 2B2	Charcot-Marie-Tooth neuropathy type 2B2; CMT2B2; C.. [+] CMT2B2; Charcot-Marie-Tooth neuropathy type 2B2; Charcot-Marie-Tooth disease neuronal type 2B2; ARCMT2B; autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2; Autosomal recessive axonal CMT4C3; 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 axonal type 2CC	Charcot-Marie-Tooth neuropathy type 2CC; CMT2CC	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 NEFH gene on chromosome 22q12. [-]
Charcot-Marie-Tooth disease axonal type 2Z	Charcot-Marie-Tooth neuropathy type 2Z; CMT2Z; aut.. [+] CMT2Z; Charcot-Marie-Tooth neuropathy type 2Z; autosomal dominant axonal Charcot-Marie-Tooth disease type 2Z [-]	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 axonal type 2C	Charcot-Marie-Tooth neuropathy type 2C; CMT2C; aut.. [+] CMT2C; Charcot-Marie-Tooth neuropathy type 2C; autosomal dominant Charcot-Marie-Tooth disease type 2C; hereditary motor and sensory neuropathy type IIc; autosomal cominant axonal Charcot-Marie-Tooth disease type 2C; HMSN2C [-]	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 TRPV4 gene on chromosome 12q24. [-]
Charcot-Marie-Tooth disease type 4C	CMT4C; Charcot-Marie-Tooth neuropathy type 4C; aut.. [+] Charcot-Marie-Tooth neuropathy type 4C; CMT4C; autosomal recessive demyelinating Charcot-Marie-Tooth disease 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 4J	CMT4J; autosomal recessive Charcot-Marie-Tooth dis.. [+] CMT4J; autosomal recessive Charcot-Marie-Tooth disease type 4J [-]	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. [-]
Charcot-Marie-Tooth disease type 4A	Charcot-Marie-Tooth neuropathy type 4A; CMT4A; aut.. [+] CMT4A; Charcot-Marie-Tooth neuropathy type 4A; 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 4D	CMT4D; Charcot-Marie-Tooth neuropathy type 4D; her.. [+] Charcot-Marie-Tooth neuropathy type 4D; CMT4D; hereditary motor and sensory neuropathy LOM type; HMSN-Lom; HMSN4D; autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D; hereditary motor abd sensory neuropathy LOM type; HMSN Lom type; HMSNL [-]	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 4K	CMT4K; autosomal recessive demyelinating Charcot-M.. [+] CMT4K; autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4K; SURF1-related Charcot-Marie-Tooth disease type 4; SURF1-related CMT4; SURF1-related severe demyelinating Charcot-Marie-Tooth disease; autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4K [-]	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 SURF1 gene on chromosome 9q34. [-]
Charcot-Marie-Tooth disease type 4B2	CMT4B2; Charcot-Marie-Tooth neuropathy type 4B2; a.. [+] Charcot-Marie-Tooth neuropathy type 4B2; CMT4B2; autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths 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 4B1	Charcot-Marie-Tooth neuropathy type 4B1; CMT4B1; a.. [+] CMT4B1; Charcot-Marie-Tooth neuropathy type 4B1; autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1 [-]	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 4H	Charcot-Marie-Tooth neuropathy type 4H; CMT4H; aut.. [+] CMT4H; Charcot-Marie-Tooth neuropathy type 4H; autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4H; 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 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 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 4E	Charcot-Marie-Tooth neuropathy type 4E; CMT4E; aut.. [+] CMT4E; Charcot-Marie-Tooth neuropathy type 4E; autosomal recessive congenital hypomyelinating or amyelinating neuropathy; Neuropathy, congenital hypomyelinating, 1 [-]	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 4G	CMT4G; Charcot-Marie-Tooth neuropathy type 4G; aut.. [+] Charcot-Marie-Tooth neuropathy type 4G; CMT4G; autosomal recessive Charcot-Marie-Tooth disease type 4G; hereditary motor and sensory neuropathy Russe type; HMSNR [-]	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 dominant intermediate B	CMTDIB; CMTDI1; Charcot-Marie-Tooth neuropathy dom.. [+] CMTDI1; CMTDIB; Charcot-Marie-Tooth neuropathy dominant intermediate B; DI-CMTB [-]	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 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 dominant intermediate C	Charcot-Marie-Tooth neuropathy dominant intermedia.. [+] Charcot-Marie-Tooth neuropathy dominant intermediate C; CMTDIC; autosomal dominant intermediate Charcot-Marie-Tooth disease type C; DI-CMTC [-]	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	CMTDID; Charcot-Marie-Tooth neuropathy dominant in.. [+] CMTDID; Charcot-Marie-Tooth neuropathy dominant intermediate D; autosomal dominant intermediate Charcot-Marie-Tooth disease type D; 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 recessive intermediate A	CMTRIA; Charcot-Marie-Tooth neuropathy recessive i.. [+] CMTRIA; Charcot-Marie-Tooth neuropathy recessive intermediate A; 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 dominant intermediate A	CMTDIA; Charcot-Marie-Tooth neuropathy dominant in.. [+] CMTDIA; Charcot-Marie-Tooth neuropathy dominant intermediate A; autosomal dominant intermediate Charcot-Marie-Tooth disease type A; DI-CMTA [-]	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 recessive intermediate D	CMTRID; autosomal recessive intermediate Charcot-M.. [+] CMTRID; autosomal recessive intermediate Charcot-Marie-Tooth disease type D; RI-CMT type D [-]	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 recessive intermediate B	Charcot-Marie-Tooth neuropathy recessive intermedi.. [+] Charcot-Marie-Tooth neuropathy recessive intermediate B; CMTRIB; autosomal recessive intermediate Charcot-Marie-Tooth disease type B; RI-CMTB [-]	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 dominant intermediate E	Charcot-Marie-Tooth neuropathy with focal segmenta.. [+] Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis; CMTDIE; Charcot-Marie-Tooth disease-nephropathy syndrome; autosomal dominant intermediate Charcot-Marie-Tooth disease type E [-]	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	CMTDIF; autosomal dominant intermediate Charcot-Ma.. [+] CMTDIF; autosomal dominant intermediate Charcot-Marie-Tooth disease type F [-]	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 X-linked dominant 6	CMT6X; CMTX6; Charcot-Marie-Tooth neuropathy X-lin.. [+] CMTX6; CMT6X; Charcot-Marie-Tooth neuropathy X-linked dominant 6; X-linked Charcot-Marie-Tooth disease type 6 [-]	A Charcot-Marie-Tooth disease X-linked that has_ma..[+] A Charcot-Marie-Tooth disease X-linked that has_material_basis_in mutation in the PDK3 gene on chromosome Xp22. [-]
Charcot-Marie-Tooth disease X-linked recessive 2	CMTX2; Charcot-Marie-Tooth neuropathy X-linked rec.. [+] CMTX2; Charcot-Marie-Tooth neuropathy X-linked recessive 2; X-linked Charcot-Marie-Tooth disease type 2 [-]	A Charcot-Marie-Tooth disease X-linked that has_ma..[+] A Charcot-Marie-Tooth disease X-linked that has_material_basis_in variation in the region Xp22.2. [-]
Charcot-Marie-Tooth disease X-linked dominant 1	CMT1X; CMTX1; Charcot-Marie-Tooth neuropathy X-lin.. [+] CMTX1; CMT1X; Charcot-Marie-Tooth neuropathy X-linked dominant 1; X-linked Charcot-Marie-Tooth disease type 1 [-]	A Charcot-Marie-Tooth disease X-linked that has_ma..[+] A Charcot-Marie-Tooth disease X-linked that has_material_basis_in hemizygous or heterozygous mutation in the GJB1 gene on chromosome Xq13. [-]	1 articles
Charcot-Marie-Tooth disease X-linked recessive 5	CMT5X; CMTX5; Charcot-Marie-Tooth neuropathy X-lin.. [+] CMTX5; CMT5X; Charcot-Marie-Tooth neuropathy X-linked recessive 5; optic atrophy, polyneuropathy, and deafness; X-linked Charcot-Marie-Tooth disease type 5; Rosenberg-Chutorian syndrome [-]	A Charcot-Marie-Tooth disease X-linked that has_ma..[+] A Charcot-Marie-Tooth disease X-linked that has_material_basis_in loss-of-function mutation in the PRPS1 gene on chromosome Xq22. [-]

???pagination.result.page??? ???pagination.result.prev??? 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 ???pagination.result.next???