Number of the records: 1
neuropatie dedičné senzorické a autonómne
SYS d009477 LBL 00000cz--a2200000n--4500 005 20250606214421.6 008 991108|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C10.500.250 065 $a C10.574.500.493 065 $a C10.668.829.800.175 065 $a C16.131.666.310 065 $a C16.320.400.415 066 $a 01 $c 03 150 $a neuropatie dedičné senzorické a autonómne $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 HSAN $2 eng 450 $w v $a HSAN Type I $2 eng 450 $w v $a HSAN Type II $2 eng 450 $w v $a HSAN Type IV $2 eng 450 $w v $a HSAN Type V $2 eng 450 $w v $a HSN Type I $2 eng 450 $w v $a HSN Type II $2 eng 450 $w v $a Insensitivity to Pain with Anhidrosis, Congenital $2 eng 450 $w v $a Neuropathies, Hereditary Sensory and Autonomic $2 eng 450 $w v $a Pain Insensitivity with Anhidrosis, Congenital $2 eng 450 $w v $a Sensory and Autonomic Neuropathies, Hereditary $2 eng 450 $w v $a Sensory Neuropathy, Hereditary $2 eng 450 $w v $a HSAN $2 slo 450 $w v $a HSAN, typ I $2 slo 450 $w v $a HSAN, typ II $2 slo 450 $w v $a HSAN, typ IV $2 slo 450 $w v $a HSAN, typ V $2 slo 450 $w v $a HSN, typ I $2 slo 450 $w v $a HSN, typ II $2 slo 450 $w v $a necitlivosť na bolesť s anhidrózou, vrodená $2 slo 450 $w v $a necitlivosť na bolesť s anhidrózou, kongenitálna $2 slo 450 $w v $a neuropatie senzorické, dedičné $2 slo 550 $7 sllk_us_auth*d000699 $Y Pain Insensitivity, Congenital $w b $a necitlivosť na bolesť, vrodená 550 $7 sllk_us_auth*d000699 $Y Pain Insensitivity, Congenital $w p $a necitlivosť na bolesť, vrodená 665 $a 2000(1989); use NEUROPATHY, HEREDITARY SENSORY 1979-1988 $2 eng 665 $a Peripheral Nerve Diseases (1966-1978) $2 eng 665 $a Peripheral Nerves (1966-1978) $2 eng 665 $a Sensation (1966-1978) $2 eng 680 9-
$i A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4) $2 eng 680 $a do not confuse with HEREDITARY SENSORY AND MOTOR NEUROPATHY; note entry terms for HSAN types: HSAN TYPE III see DYSAUTONOMIA, FAMILIAL is also available $2 eng 750 -2
$a Hereditary Sensory and Autonomic Neuropathies $2 eng 980 $x M
Number of the records: 1