loading...| Preferred Name |
Hereditary Sensory and Autonomic Neuropathies [Disease/Finding] |
|
| Synonyms |
Sensory and Autonomic Neuropathies, Hereditary HSAN (Hereditary Sensory Autonomic Neuropathy) |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002179 |
|
| altLabel |
Sensory and Autonomic Neuropathies, Hereditary Hereditary Sensory and Autonomic Neuropathies Neuropathies, Hereditary Sensory and Autonomic HSAN HSAN (Hereditary Sensory Autonomic Neuropathy) |
|
| cui |
C0027889 |
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| MESH DEFINITION |
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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| MESH DUI |
D009477 |
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| MeSH name |
Hereditary Sensory and Autonomic Neuropathies |
|
| MESH UI |
M0014743 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000002179 |
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| NUI |
N0000002179 |
|
| prefLabel |
Hereditary Sensory and Autonomic Neuropathies [Disease/Finding] |
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| SNOMED CID |
128205005 |
|
| tui |
T047 |
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| subClassOf |