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Medical Subject Headings
Preferred Name | Amyloid Neuropathies | |
Synonyms |
Neuropathy, Amyloid Neuropathy, Secondary Amyloid Amyloid Neuropathy Secondary Amyloid Neuropathy Amyloid Neuropathies, Secondary Polyneuropathy, Amyloid Amyloid Polyneuropathies Neuropathies, Amyloid Polyneuropathies, Amyloid Amyloid Neuropathy, Secondary Neuropathies, Secondary Amyloid Amyloid Polyneuropathy Secondary Amyloid Neuropathies |
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Definitions |
Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349) |
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ID |
http://purl.bioontology.org/ontology/MESH/D017772 |
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altLabel |
Neuropathy, Amyloid Neuropathy, Secondary Amyloid Amyloid Neuropathy Secondary Amyloid Neuropathy Amyloid Neuropathies, Secondary Polyneuropathy, Amyloid Amyloid Polyneuropathies Neuropathies, Amyloid Polyneuropathies, Amyloid Amyloid Neuropathy, Secondary Neuropathies, Secondary Amyloid Amyloid Polyneuropathy Secondary Amyloid Neuropathies
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AN |
coord IM with specific neurol dis (IM) or specific nerve (IM); /genet: consider also AMYLOID NEUROPATHIES, FAMILIAL
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AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
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cui |
C0206247 C0751660
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DC |
1
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definition |
Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349)
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DX |
19940101
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HN |
1994
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Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
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Machine permutation |
1994
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Mapped from | ||
MDA |
19930630
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MMR |
20090706
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MN |
C10.668.829.050 C18.452.845.500.050
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notation |
D017772
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prefLabel |
Amyloid Neuropathies
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TERMUI |
T053184 T369830 T053183 T053185
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TH |
NLM (2000) NLM (1994) ORD (2010)
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tui |
T047
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subClassOf |
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