| Descriptor English: | Dysautonomia, Familial | ||||||
| Descriptor Spanish: |
Disautonomía Familiar
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| Descriptor Portuguese: | Disautonomia Familiar | ||||||
| Descriptor French: | Dysautonomie familiale | ||||||
| Entry term(s): |
Dominant Hereditary Sensory Neuropathy, Type III Familial Dysautonomia HSAN (Hereditary Sensory and Autonomic Neuropathy) Type III HSAN 3 HSAN III HSAN Type III HSAN3 HSN-III Hereditary Sensory Neuropathy Type 3 Hereditary Sensory Neuropathy, Dominant, Type 3 Hereditary Sensory Neuropathy, Dominant, Type III Hereditary Sensory Neuropathy, Type 3, Dominant Hereditary Sensory and Autonomic Neuropathy 3 Hereditary Sensory and Autonomic Neuropathy Type III Hereditary-Sensory and Autonomic Neuropathy Type III Neuropathy, Hereditary Sensory And Autonomic, Type III Neuropathy, Hereditary and Autonomic, Type III Riley Day Syndrome Riley-Day Syndrome Type 3 Hereditary Sensory Neuropathy, Dominant Type III Hereditary Sensory Neuropathy, Dominant |
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| Tree number(s): |
C10.177.575.300 C10.500.250.309 C10.574.500.493.250 C10.668.829.800.175.250 C16.131.666.310.309 C16.320.400.415.309 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D004402 | ||||||
| Scope note: | An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations are present at birth and include diminished lacrimation, defective thermoregulation, orthostatic hypotension (HYPOTENSION, ORTHOSTATIC), fixed pupils, excessive SWEATING, loss of pain and temperature sensation, and absent reflexes. Pathologic features include reduced numbers of small diameter peripheral nerve fibers and autonomic ganglion neurons. (From Adams et al., Principles of Neurology, 6th ed, p1348; Nat Genet 1993;4(2):160-4) |
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| Annotation: | PRIMARY DYSAUTONOMIAS is also available |
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| 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 |
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| Public MeSH Note: | 1981; see AUTONOMIC DYSFUNCTION 1963-1980 |
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| History Note: | 1981; uss AUTONOMIC DYSFUNCTION 1963-1980 |
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| DeCS ID: | 23989 | ||||||
| Unique ID: | D004402 | ||||||
| NLM Classification: | WL 600 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1981/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2018/06/30 |
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Dysautonomia, Familial
- Preferred
| Concept UI |
M0006912 |
| Scope note | An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations are present at birth and include diminished lacrimation, defective thermoregulation, orthostatic hypotension (HYPOTENSION, ORTHOSTATIC), fixed pupils, excessive SWEATING, loss of pain and temperature sensation, and absent reflexes. Pathologic features include reduced numbers of small diameter peripheral nerve fibers and autonomic ganglion neurons. (From Adams et al., Principles of Neurology, 6th ed, p1348; Nat Genet 1993;4(2):160-4) |
| Preferred term | Dysautonomia, Familial |
| Entry term(s) |
Dominant Hereditary Sensory Neuropathy, Type III Familial Dysautonomia HSAN (Hereditary Sensory and Autonomic Neuropathy) Type III HSAN 3 HSAN III HSAN Type III HSAN3 HSN-III Hereditary Sensory Neuropathy Type 3 Hereditary Sensory Neuropathy, Dominant, Type 3 Hereditary Sensory Neuropathy, Dominant, Type III Hereditary Sensory Neuropathy, Type 3, Dominant Hereditary Sensory and Autonomic Neuropathy 3 Hereditary Sensory and Autonomic Neuropathy Type III Hereditary-Sensory and Autonomic Neuropathy Type III Neuropathy, Hereditary Sensory And Autonomic, Type III Neuropathy, Hereditary and Autonomic, Type III Riley Day Syndrome Riley-Day Syndrome Type 3 Hereditary Sensory Neuropathy, Dominant Type III Hereditary Sensory Neuropathy, Dominant |
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