Number of the records: 1
neuropatie dedičné senzorické a autonómne
Record number d009477 Date 06.06.2025 Type M - MESH Topical term neuropatie dedičné senzorické a autonómne Other term English (Pseudonym) HSAN
English (Pseudonym) HSAN Type I
English (Pseudonym) HSAN Type II
English (Pseudonym) HSAN Type IV
English (Pseudonym) HSAN Type V
English (Pseudonym) HSN Type I
English (Pseudonym) HSN Type II
English (Pseudonym) Insensitivity to Pain with Anhidrosis, Congenital
English (Pseudonym) Neuropathies, Hereditary Sensory and Autonomic
English (Pseudonym) Pain Insensitivity with Anhidrosis, Congenital
English (Pseudonym) Sensory and Autonomic Neuropathies, Hereditary
English (Pseudonym) Sensory Neuropathy, Hereditary
Slovak (Pseudonym) HSAN
Slovak (Pseudonym) HSAN, typ I
Slovak (Pseudonym) HSAN, typ II
Slovak (Pseudonym) HSAN, typ IV
Slovak (Pseudonym) HSAN, typ V
Slovak (Pseudonym) HSN, typ I
Slovak (Pseudonym) HSN, typ II
Slovak (Pseudonym) necitlivosť na bolesť s anhidrózou, vrodená
Slovak (Pseudonym) necitlivosť na bolesť s anhidrózou, kongenitálna
Slovak (Pseudonym) neuropatie senzorické, dedičné
See also (Later heading) necitlivosť na bolesť, vrodená
(Skutočné meno) necitlivosť na bolesť, vrodená
UDC C10.500.250C10.574.500.493C10.668.829.800.175C16.131.666.310C16.320.400.415 Note 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) 
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Number of the records: 1