Concept information
Nervous System Diseases
Neuromuscular Diseases
Peripheral Nervous System Diseases
Amyloid Neuropathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amyloidosis, Familial
Preferred term
Amyloid Neuropathies, Familial
Type
-
Topical Descriptor
Broader concept
Entry terms
- Amyloidoses, Hereditary Neuropathic
- Amyloidosis, Hereditary Neuropathic
- Amyloid Polyneuropathies, Familial
- Amyloid Polyneuropathy, Familial
- Familial Amyloid Polyneuropathies
- Familial Amyloid Polyneuropathy
- Hereditary Neuropathic Amyloidoses
- Hereditary Neuropathic Amyloidosis
- Neuropathic Amyloidoses, Hereditary
- Neuropathic Amyloidosis, Hereditary
- Polyneuropathies, Familial Amyloid
- Polyneuropathy, Familial Amyloid
Scope note
- Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.
History note
- 2002; use AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES use AMYLOID NEUROPATHIES 1994-2001
In other languages
-
Finnish
-
familiaalinen amyloidineuropatia
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familiaaliset amyloidineuropatiat
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familiaarinen amyloidineuropatia
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familiaariset amyloidineuropatiat
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suvuittainen amyloidineuropatia
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Swedish
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Familjär amyloidos med polyneuropati
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Skelleftesjukan
-
Wohlwill–Corino-Andrades syndrom
-
Ärftlig transtyretinamyloidos
URI
http://www.yso.fi/onto/mesh/D028227
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