Related MeSH Hierarchy (7)
Diseases [C] » Nervous System Diseases [C10] » Neurodegenerative Diseases » Heredodegenerative Disorders, Nervous System » Amyloid Neuropathies, Familial
Diseases [C] » Nervous System Diseases [C10] » Neuromuscular Diseases » Peripheral Nervous System Diseases » Amyloid Neuropathies » Amyloid Neuropathies, Familial
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Heredodegenerative Disorders, Nervous System » Amyloid Neuropathies, Familial
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Amyloidosis, Familial » Amyloid Neuropathies, Familial
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Amyloidosis, Familial » Amyloid Neuropathies, Familial
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Proteostasis Deficiencies » Amyloidosis » Amyloid Neuropathies » Amyloid Neuropathies, Familial
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Proteostasis Deficiencies » Amyloidosis » Amyloidosis, Familial » Amyloid Neuropathies, Familial
Description
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. MeSH
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Approved Indicated Drugs (4)
Phase 3 Indicated Drugs (3)
Organization Involved with Phase 3 Indications (8)
Organization Involved with Phase 2 Indications (3)
Organization Involved with Phase 1 Indications (1)
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UMLS Data
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