Number of the records: 1
neuropatie dedičné senzorické a motorické
SYS d015417 LBL 00000cz--a2200000n--4500 005 20250606213112.4 008 991108|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 $a BA006 $d BA006 $d BA006 065 $a C10.500.300 065 $a C10.574.500.495 065 $a C10.668.829.800.300 065 $a C16.131.666.300 065 $a C16.320.400.375 066 $a 01 $c 03 150 $a neuropatie dedičné senzorické a motorické $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $2 slo 450 $w v $a Déjerineov-Sottasov syndróm $2 slo 450 $w v $a Déjerineova-Sottasova choroba $2 slo 450 $w v $a Déjerineova-Sottasova neuropatia $2 slo 450 $w v $a Déjerineova-Sottasova hypertrofická neuropatia $2 slo 450 $w v $a neuropatie dedičné motorické a senzorické $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická 3 $2 slo 450 $w v $a neuropatie hereditárne motorické a senzorické $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická, typ VII $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická, typ III $2 slo 450 $w v $a neuropatia proximálna dedičná motorická, typ I $2 slo 450 $w v $a HMSN $2 slo 450 $w v $a HMSN, typ III $2 slo 450 $w v $a HMSN, typ VII $2 slo 450 $w v $a HMSN3 $2 slo 450 $w v $a CMT4f $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, demyelinizačný typ 4f $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, typ 3 $2 slo 665 $a 2000(1989); for HMN (HEREDITARY MOTOR NEUROPATHY) PROXIMAL TYPE I use SPINAL MUSCULAR ATROPHIES OF CHILDHOOD 1988-2025 $2 eng 665 $a Charcot-Marie Disease (1975-1988) $2 eng 665 $a Muscular Atrophy (1972-1988) $2 eng 665 $a Neuromuscular Diseases (1979-1988) $2 eng 680 9-
$i A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343) $2 eng 680 $a do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES $2 eng 750 -2
$a Hereditary Sensory and Motor Neuropathy $2 eng 980 $x M
Number of the records: 1