Search on: INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS 
Descriptors Found: 1
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Descriptor English:   Hereditary Sensory and Autonomic Neuropathies 
Descriptor Spanish:   Neuropatías Hereditarias Sensoriales y Autónomas 
Descriptor Portuguese:   Neuropatias Hereditárias Sensoriais e Autônomas 
Synonyms English:   Acroosteolysis, Giaccai Type
Acroosteolysis, Neurogenic
Congenital Insensitivity to Pain with Anhidrosis
Familial Dysautonomia, Type 2
Familial Dysautonomia, Type II
Giaccai Type Acroosteolysis
HSAN (Hereditary Sensory Autonomic Neuropathy)
HSAN 1
HSAN 4
HSAN 5
HSAN I
HSAN IV
HSAN V
HSAN2
HSAN5
HSANII
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 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, Congenital, with Anhidrosis
Neurogenic Acroosteolysis
Neuropathy Hereditary Sensory Radicular, Autosomal Dominant
Neuropathy Hereditary Sensory and Autonomic Type 1
Neuropathy, Congenital Sensory
Neuropathy, Congenital Sensory, with Anhidrosis
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
Acroosteolyses, Neurogenic
Congenital Sensory Neuropathies
Congenital Sensory Neuropathy
HSANs (Hereditary Sensory Autonomic Neuropathy)
HSN Type IIs
Hereditary Sensory Neuropathies
Hereditary Sensory Neuropathy
Neurogenic Acroosteolyses
Neuropathies, Congenital Sensory
Neuropathies, Hereditary Sensory
Neuropathy, Hereditary Sensory
Sensory Neuropathies, Congenital
Sensory Neuropathies, Hereditary
Sensory Neuropathy, Congenital
Type I, HSAN
Type I, HSN
Type IV, HSAN
Neuropathies, Hereditary Sensory and Autonomic
HSAN
HSAN Type I
HSAN Type II
HSAN Type IV
HSAN Type V
HSN Type I
HSN Type II
Sensory and Autonomic Neuropathies, Hereditary
Sensory Neuropathy, Hereditary
Insensitivity to Pain with Anhidrosis, Congenital
Pain Insensitivity with Anhidrosis, Congenital  
Tree Number:   C10.500.310
C10.574.500.496
C10.668.829.800.175
C16.131.666.310
C16.320.400.415
Definition English:   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) 
Indexing Annotation English:   do not confuse with HEREDITARY SENSORY AND MOTOR NEUROPATHY; note entry terms for HSAN types: HSAN TYPE III see DYSAUTONOMIA, FAMILIAL is also available
See Related English:   Pain Insensitivity, Congenital
 
History Note English:   2000(1989); use NEUROPATHY, HEREDITARY SENSORY 1979-1988 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   23938 
Unique Identifier:   D009477 

Occurrence in VHL:
 

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