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#613353 - MONONEUROPATHY OF THE MEDIAN NERVE, MILD; MNMN
Cytogenetic locations: 606331
Gene summaries Genetic tests Medical literature
#115430 - CARPAL TUNNEL SYNDROME 1; CTS1
CARPAL TUNNEL SYNDROME, INCLUDED; CTS, INCLUDED
Cytogenetic locations: 19444109
#619161 - CARPAL TUNNEL SYNDROME 2; CTS2
Cytogenetic locations: 611340
*600310 - CARTILAGE OLIGOMERIC MATRIX PROTEIN; COMP
Cytogenetic locations: Cyclin-dependent
*176300 - TRANSTHYRETIN; TTR
Cytogenetic locations: 19547003
#607016 - SCHEIE SYNDROME
Cytogenetic locations: 619327
#607014 - HURLER SYNDROME
#105210 - AMYLOIDOSIS, HEREDITARY SYSTEMIC 1; AMYLD1
Cytogenetic locations: 610117
#252600 - MUCOLIPIDOSIS III ALPHA/BETA
MUCOLIPIDOSIS III ALPHA/BETA, ATYPICAL, INCLUDED
Cytogenetic locations: 18131303
#620683 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 9; FPLD9
#253200 - MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6
Cytogenetic locations: 26776877
*608206 - SH3 DOMAIN AND TETRATRICOPEPTIDE REPEAT DOMAIN 2; SH3TC2
Cytogenetic locations: 14574644
156220 - MERALGIA PARAESTHETICA, FAMILIAL
*134934 - FIBROBLAST GROWTH FACTOR RECEPTOR 3; FGFR3
FGFR3/TACC3 FUSION GENE, INCLUDED
Cytogenetic locations: 18076102
*109700 - BETA-2-MICROGLOBULIN; B2M
Cytogenetic locations: 608145
#162500 - NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP
Cytogenetic locations: 612341
#620659 - AMYLOIDOSIS, HEREDITARY SYSTEMIC 6; AMYLD6
#132400 - EPIPHYSEAL DYSPLASIA, MULTIPLE, 1; EDM1
EPIPHYSEAL DYSPLASIA, FAIRBANK TYPE, INCLUDED
#610250 - SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31
Cytogenetic locations: 16826527
#101800 - ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1
Cytogenetic locations: 610904
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