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Descriptor English: Hereditary Sensory and Autonomic Neuropathies
Descriptor Spanish: Neuropatías Hereditarias Sensoriales y Autónomas
Descriptor neuropatías hereditarias sensitivas y autónomas
Entry term(s) HSAN
HSAN de tipo I
HSAN de tipo II
HSAN de tipo IV
HSAN de tipo V
HSN de tipo I
HSN de tipo II
insensibilidad congénita al dolor con anhidrosis
neuropatía sensitiva hereditaria
neuropatías autónomas y sensitivas hereditarias
neuropatías hereditarias sensoriales y autónomas
neuropatías sensoriales y autónomas hereditarias
Scope note: Grupo de trastornos hereditarios caracterizados por degeneración de las raíces dorsales y de las células ganglionares autónomas, y clínicamente por la pérdida sensitiva y disfunción autónoma. Hay cinco subtipos. El tipo I se caracteriza por herencia autosómica dominante y afectación sensitiva distal. El tipo II caracterizado por herencia autosómica y pérdida sensitiva distal y proximal. El tipo III es la DISAUTONOMÍA, FAMILIAR. El tipo IV se caracteriza por insensibilidad al dolor, intolerancia al calor, y deficiencia mental. El tipo V se caracteriza por pérdida selectiva del dolor con sensibilidad intacta a las sensaciones tactiles ligeras y a las vibraciones. (Joynt, Clinical Neurology, 1995, Ch51, pp142-4)
Descriptor Portuguese: Neuropatias Hereditárias Sensoriais e Autônomas
Descriptor French: Neuropathies héréditaires sensitives et autonomes
Entry term(s): Acroosteolyses, Neurogenic
Acroosteolysis, Giaccai Type
Acroosteolysis, Neurogenic
Congenital Insensitivity to Pain with Anhidrosis
Congenital Sensory Neuropathies
Congenital Sensory Neuropathy
Familial Dysautonomia, Type 2
Familial Dysautonomia, Type II
Giaccai Type Acroosteolysis
HSAN
HSAN (Hereditary Sensory Autonomic Neuropathy)
HSAN 1
HSAN 4
HSAN 5
HSAN I
HSAN IV
HSAN Type I
HSAN Type II
HSAN Type IV
HSAN Type V
HSAN V
HSAN2
HSAN5
HSANII
HSANs (Hereditary Sensory Autonomic Neuropathy)
HSN Type I
HSN Type II
HSN Type IIs
Hereditary Sensory And Autonomic Neuropathy IV
Hereditary Sensory Autonomic Neuropathy, Type 1
Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 4
Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Neuropathies
Hereditary Sensory Neuropathy
Hereditary Sensory Neuropathy Type 1
Hereditary Sensory Neuropathy Type I
Hereditary Sensory Neuropathy Type Ia
Hereditary Sensory Radicular Neuropathy
Hereditary Sensory Radicular Neuropathy, Recessive Form
Hereditary Sensory and Autonomic Neuropathy 4
Hereditary Sensory and Autonomic Neuropathy Type 1
Hereditary Sensory and Autonomic Neuropathy Type 2
Hereditary Sensory and Autonomic Neuropathy Type I
Hereditary Sensory and Autonomic Neuropathy Type II
Hereditary Sensory and Autonomic Neuropathy Type IV
Hereditary Sensory and Autonomic Neuropathy Type V
Hereditary Sensory and Autonomic Neuropathy, Type 4
Hereditary Sensory and Autonomic Neuropathy, Type 5
Insensitivity to Pain with Anhidrosis, Congenital
Insensitivity to Pain, Congenital, with Anhidrosis
Neurogenic Acroosteolyses
Neurogenic Acroosteolysis
Neuropathies, Congenital Sensory
Neuropathies, Hereditary Sensory
Neuropathies, Hereditary Sensory and Autonomic
Neuropathy Hereditary Sensory Radicular, Autosomal Dominant
Neuropathy Hereditary Sensory and Autonomic Type 1
Neuropathy, Congenital Sensory
Neuropathy, Congenital Sensory, with Anhidrosis
Neuropathy, Hereditary Sensory
Neuropathy, Hereditary Sensory And Autonomic, Type I
Neuropathy, Hereditary Sensory And Autonomic, Type V
Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant
Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive
Neuropathy, Hereditary Sensory, Type I
Neuropathy, Progressive Sensory, Of Children
Pain Insensitivity with Anhidrosis, Congenital
Sensory Neuropathies, Congenital
Sensory Neuropathies, Hereditary
Sensory Neuropathy, Congenital
Sensory Neuropathy, Hereditary
Sensory and Autonomic Neuropathies, Hereditary
Type I, HSAN
Type I, HSN
Type IV, HSAN
Tree number(s): C10.500.250
C10.574.500.493
C10.668.829.800.175
C16.131.666.310
C16.320.400.415
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D009477
Scope 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)
Annotation: do not confuse with HEREDITARY SENSORY AND MOTOR NEUROPATHY; note entry terms for HSAN types: HSAN TYPE III see DYSAUTONOMIA, FAMILIAL is also available
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Peripheral Nerve Diseases (1966-1978)
Peripheral Nerves (1966-1978)
Sensation (1966-1978)
Public MeSH Note: 2000; see NEUROPATHIES, HEREDITARY SENSORY AND AUTONOMIC 1989-1999; see NEUROPATHY, HEREDITARY SENSORY 1979-1988
History Note: 2000(1989); use NEUROPATHY, HEREDITARY SENSORY 1979-1988
Entry Version: HEREDITARY SENSORY AUTONOMIC NEUROPATHIES
Related: Pain Insensitivity, Congenital MeSH
DeCS ID: 23938
Unique ID: D009477
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1979/01/01
Date of Entry: 1999/11/08
Revision Date: 2018/06/30
Hereditary Sensory and Autonomic Neuropathies - Preferred
Concept UI M0014743
Scope 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)
Preferred term Hereditary Sensory and Autonomic Neuropathies
Entry term(s) HSAN
HSAN (Hereditary Sensory Autonomic Neuropathy)
HSANs (Hereditary Sensory Autonomic Neuropathy)
Neuropathies, Hereditary Sensory and Autonomic
Sensory and Autonomic Neuropathies, Hereditary
Hereditary Sensory and Autonomic Neuropathy Type V - Narrower
Concept UI M0583610
Preferred term Hereditary Sensory and Autonomic Neuropathy Type V
Entry term(s) HSAN 5
HSAN Type V
HSAN V
HSAN5
Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory and Autonomic Neuropathy, Type 5
Neuropathy, Hereditary Sensory And Autonomic, Type V
Hereditary Sensory Neuropathy Type I - Narrower
Concept UI M0583611
Preferred term Hereditary Sensory Neuropathy Type I
Entry term(s) HSAN 1
HSAN I
HSAN Type I
HSN Type I
Hereditary Sensory Autonomic Neuropathy, Type 1
Hereditary Sensory Neuropathy Type 1
Hereditary Sensory Neuropathy Type Ia
Hereditary Sensory and Autonomic Neuropathy Type 1
Hereditary Sensory and Autonomic Neuropathy Type I
Neuropathy Hereditary Sensory Radicular, Autosomal Dominant
Neuropathy Hereditary Sensory and Autonomic Type 1
Neuropathy, Hereditary Sensory And Autonomic, Type I
Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant
Neuropathy, Hereditary Sensory, Type I
Type I, HSAN
Type I, HSN
HSAN Type IV - Narrower
Concept UI M0014741
Preferred term HSAN Type IV
Entry term(s) Congenital Insensitivity to Pain with Anhidrosis
Familial Dysautonomia, Type 2
Familial Dysautonomia, Type II
HSAN 4
HSAN IV
Hereditary Sensory And Autonomic Neuropathy IV
Hereditary Sensory Autonomic Neuropathy, Type 4
Hereditary Sensory and Autonomic Neuropathy 4
Hereditary Sensory and Autonomic Neuropathy Type IV
Hereditary Sensory and Autonomic Neuropathy, Type 4
Insensitivity to Pain with Anhidrosis, Congenital
Insensitivity to Pain, Congenital, with Anhidrosis
Neuropathy, Congenital Sensory, with Anhidrosis
Pain Insensitivity with Anhidrosis, Congenital
Type IV, HSAN
Sensory Neuropathy, Hereditary - Narrower
Concept UI M0014745
Preferred term Sensory Neuropathy, Hereditary
Entry term(s) Acroosteolyses, Neurogenic
Acroosteolysis, Neurogenic
Congenital Sensory Neuropathies
Congenital Sensory Neuropathy
Hereditary Sensory Neuropathies
Hereditary Sensory Neuropathy
Neurogenic Acroosteolyses
Neurogenic Acroosteolysis
Neuropathies, Congenital Sensory
Neuropathies, Hereditary Sensory
Neuropathy, Congenital Sensory
Neuropathy, Hereditary Sensory
Sensory Neuropathies, Congenital
Sensory Neuropathies, Hereditary
Sensory Neuropathy, Congenital
Hereditary Sensory and Autonomic Neuropathy Type II - Narrower
Concept UI M0583609
Preferred term Hereditary Sensory and Autonomic Neuropathy Type II
Entry term(s) Acroosteolysis, Giaccai Type
Giaccai Type Acroosteolysis
HSAN Type II
HSAN2
HSANII
HSN Type II
HSN Type IIs
Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Radicular Neuropathy, Recessive Form
Hereditary Sensory and Autonomic Neuropathy Type 2
Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive
Neuropathy, Progressive Sensory, Of Children
Hereditary Sensory Radicular Neuropathy - Narrower
Concept UI M0014744
Preferred term Hereditary Sensory Radicular Neuropathy



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