Next Generation Sequencing Competence Network

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)

Descriptor ID	D009477
MeSH Number(s)	C10.500.310 C10.574.500.496 C10.668.829.800.175 C16.131.666.310 C16.320.400.415
Concept/Terms	Hereditary Sensory and Autonomic Neuropathies Hereditary Sensory and Autonomic Neuropathies Sensory and Autonomic Neuropathies, Hereditary Neuropathies, Hereditary Sensory and Autonomic HSAN HSAN (Hereditary Sensory Autonomic Neuropathy) HSANs (Hereditary Sensory Autonomic Neuropathy) Hereditary Sensory and Autonomic Neuropathy Type V Hereditary Sensory and Autonomic Neuropathy Type V Hereditary Sensory Autonomic Neuropathy, Type 5 Neuropathy, Hereditary Sensory And Autonomic, Type V HSAN Type V HSAN V HSAN5 Hereditary Sensory and Autonomic Neuropathy, Type 5 HSAN 5 Hereditary Sensory Neuropathy Type I Hereditary Sensory Neuropathy Type I Hereditary Sensory and Autonomic Neuropathy Type I Hereditary Sensory Autonomic Neuropathy, Type 1 Hereditary Sensory Neuropathy Type 1 Hereditary Sensory Neuropathy Type Ia HSAN 1 HSAN I HSAN Type I Type I, HSAN HSN Type I Type I, HSN Neuropathy Hereditary Sensory and Autonomic Type 1 Neuropathy Hereditary Sensory Radicular, Autosomal Dominant Neuropathy, Hereditary Sensory And Autonomic, Type I Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant Neuropathy, Hereditary Sensory, Type I Hereditary Sensory and Autonomic Neuropathy Type 1 HSAN Type IV HSAN Type IV Type IV, HSAN Familial Dysautonomia, Type 2 Familial Dysautonomia, Type II Hereditary Sensory and Autonomic Neuropathy 4 Hereditary Sensory And Autonomic Neuropathy IV Hereditary Sensory and Autonomic Neuropathy Type IV Hereditary Sensory and Autonomic Neuropathy, Type 4 Hereditary Sensory Autonomic Neuropathy, Type 4 HSAN 4 HSAN IV Insensitivity to Pain with Anhidrosis, Congenital Insensitivity to Pain, Congenital, with Anhidrosis Neuropathy, Congenital Sensory, with Anhidrosis Pain Insensitivity with Anhidrosis, Congenital Congenital Insensitivity to Pain with Anhidrosis Sensory Neuropathy, Hereditary Sensory Neuropathy, Hereditary Hereditary Sensory Neuropathies Hereditary Sensory Neuropathy Neuropathies, Hereditary Sensory Neuropathy, Hereditary Sensory Sensory Neuropathies, Hereditary Neurogenic Acroosteolysis Neuropathy, Congenital Sensory Congenital Sensory Neuropathies Congenital Sensory Neuropathy Neuropathies, Congenital Sensory Sensory Neuropathies, Congenital Sensory Neuropathy, Congenital Acroosteolysis, Neurogenic Acroosteolyses, Neurogenic Neurogenic Acroosteolyses Hereditary Sensory and Autonomic Neuropathy Type II Hereditary Sensory and Autonomic Neuropathy Type II Giaccai Type Acroosteolysis Hereditary Sensory and Autonomic Neuropathy Type 2 Hereditary Sensory Autonomic Neuropathy, Type 2 Neuropathy, Progressive Sensory, Of Children HSAN Type II HSAN2 HSANII HSN Type II HSN Type IIs Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive Acroosteolysis, Giaccai Type Hereditary Sensory Radicular Neuropathy, Recessive Form Hereditary Sensory Radicular Neuropathy Hereditary Sensory Radicular Neuropathy

Below are MeSH descriptors whose meaning is more general than "Hereditary Sensory and Autonomic Neuropathies".

Below are MeSH descriptors whose meaning is related to "Hereditary Sensory and Autonomic Neuropathies".

Below are MeSH descriptors whose meaning is more specific than "Hereditary Sensory and Autonomic Neuropathies".