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 DeCS Categories

C10 Nervous System Diseases .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.050 Amyloid Neuropathies, Familial .
C10.668 Neuromuscular Diseases .
C10.668.829 Peripheral Nervous System Diseases .
C10.668.829.050 Amyloid Neuropathies .
C10.668.829.050.050 Amyloid Neuropathies, Familial .
C10.668.829.100 Brachial Plexus Neuropathies .
C10.668.829.100.500 Brachial Plexus Neuritis .
C10.668.829.650 Neuritis .
C10.668.829.650.250 Brachial Plexus Neuritis .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.050 Amyloid Neuropathies, Familial .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.176 Amyloidosis, Familial .
C16.320.565.176.050 Amyloid Neuropathies, Familial .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.176 Amyloidosis, Familial .
C18.452.648.176.050 Amyloid Neuropathies, Familial .
C18.452.845 Proteostasis Deficiencies .
C18.452.845.500 Amyloidosis .
C18.452.845.500.050 Amyloid Neuropathies .
C18.452.845.500.050.050 Amyloid Neuropathies, Familial .
C18.452.845.500.075 Amyloidosis, Familial .
C18.452.845.500.075.050 Amyloid Neuropathies, Familial .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.742 Pyrimidines .
D03.383.742.698 Pyrimidinones .
D03.383.742.698.253 Barbiturates .
D03.383.742.698.253.077 Amobarbital .
D06 Hormones, Hormone Substitutes, and Hormone Antagonists .
D06.472 Hormones .
D06.472.699 Peptide Hormones .
D06.472.699.587 Pancreatic Hormones .
D06.472.699.587.334 Islet Amyloid Polypeptide .
D12 Amino Acids, Peptides, and Proteins .
D12.644 Peptides .
D12.644.548 Peptide Hormones .
D12.644.548.586 Pancreatic Hormones .
D12.644.548.586.234 Islet Amyloid Polypeptide .
D12.776 Proteins .
D12.776.049 Amyloid .
D12.776.049.407 Amyloidogenic Proteins .
D12.776.049.407.500 Islet Amyloid Polypeptide .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Amobarbital .
Amobarbital Sodium .
Amsal .
Amylbarb sodium .
Amylobeta .
Amytal .
Amytal Sodium .
Barbamyl .
Eunoctal .
Isoamitil Sedante .
Isonal .
Neur-Amyl .
Novamobarb .
Placidel .
Sodium Amobarbital .
Sodium Amytal .
Transital .
Amobarbital, Sodium .
Sodium, Amobarbital .
Amylobarbitone .
Pentymal .
BARBAMYL .
A barbiturate with hypnotic and sedative properties (but not antianxiety). Adverse effects are mainly a consequence of dose-related CNS depression and the risk of dependence with continued use is high. (From Martindale, The Extra Pharmacopoeia, 30th ed, p565) .
1.00
81937
 
Amyloid Neuropathies .
Amyloid Neuropathy, Secondary .
Amyloid Polyneuropathies .
Amyloid Neuropathies, Secondary .
Amyloid Neuropathy .
Amyloid Polyneuropathy .
Neuropathies, Secondary Amyloid .
Neuropathy, Amyloid .
Neuropathy, Secondary Amyloid .
Polyneuropathies, Amyloid .
Polyneuropathy, Amyloid .
Secondary Amyloid Neuropathies .
Secondary Amyloid Neuropathy .
Neuropathies, Amyloid .
AMYLOID POLYNEUROPATHIES .
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) .
0.77
9541
 
Amyloid Neuropathies, Familial .
Amyloid Neuropathy Type 1 .
Amyloid Polyneuropathy, British Type .
Amyloid Polyneuropathy, Iowa Type .
Amyloid Polyneuropathy, Swiss Type .
Appalachian Type Familial Amyloid Polyneuropathy .
British Type Amyloid Polyneuropathy .
Familial Amyloid Neuropathy, Andrade Type .
Familial Amyloid Neuropathy, Finnish Type .
Familial Amyloid Neuropathy, Portuguese Type .
Familial Amyloid Polyneuropathy, Appalachian Type .
Familial Amyloid Polyneuropathy, Jewish Type .
Familial Amyloid Polyneuropathy, Type I .
Familial Amyloid Polyneuropathy, Type II .
Familial Amyloid Polyneuropathy, Type III .
Familial Amyloid Polyneuropathy, Type IV .
Familial Amyloid Polyneuropathy, Type V .
Familial Amyloid Polyneuropathy, Type VI .
Familial Portuguese Polyneuritic Amyloidosis .
Finnish Type Familial Amyloid Neuropathy .
Hereditary Neuropathic Amyloidosis .
Iowa Type Amyloid Polyneuropathy .
Jewish Type Familial Amyloid Polyneuropathy .
Neuropathic Amyloid Syndrome .
Polyneuritic Amyloidosis, Portuguese .
Portuguese Polyneuritic Amyloidosis .
Portuguese Type Familial Amyloid Neuropathy .
Swiss Type Amyloid Polyneuropathy .
Type I Familial Amyloid Polyneuropathy .
Type II Familial Amyloid Polyneuropathy .
Type III Familial Amyloid Polyneuropathy .
Type IV Familial Amyloid Polyneuropathy .
Type V Familial Amyloid Polyneuropathy .
Type VI Familial Amyloid Polyneuropathy .
Wohlwill-Andrade Syndrome .
Wohlwill-Corino Andrade Syndrome .
Amyloid Neuropathy, Familial .
Amyloid Polyneuropathies, Familial .
Amyloid Polyneuropathy, Familial .
Amyloid Syndrome, Neuropathic .
Amyloid Syndromes, Neuropathic .
Amyloidoses, Hereditary Neuropathic .
Amyloidoses, Portuguese Polyneuritic .
Amyloidosis, Hereditary Neuropathic .
Amyloidosis, Portuguese Polyneuritic .
Familial Amyloid Neuropathies .
Familial Amyloid Neuropathy .
Familial Amyloid Polyneuropathy .
Hereditary Neuropathic Amyloidoses .
Neuropathic Amyloid Syndromes .
Neuropathic Amyloidoses, Hereditary .
Neuropathic Amyloidosis, Hereditary .
Neuropathies, Familial Amyloid .
Neuropathy, Familial Amyloid .
Polyneuritic Amyloidoses, Portuguese .
Polyneuropathies, Familial Amyloid .
Polyneuropathy, Familial Amyloid .
Portuguese Polyneuritic Amyloidoses .
Syndrome, Neuropathic Amyloid .
Syndrome, Wohlwill-Andrade .
Syndrome, Wohlwill-Corino Andrade .
Syndromes, Neuropathic Amyloid .
Wohlwill Andrade Syndrome .
Wohlwill Corino Andrade Syndrome .
Familial Amyloid Polyneuropathies .
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. .
0.65
9848
 
Brachial Plexus Neuritis .
Amyotrophic Neuralgia .
Amyotrophy, Hereditary Neuralgic .
Amyotrophy, Hereditary Neuralgic, with Predilection for Brachial Plexus .
Brachial Neuralgia .
Brachial Neuritis .
Brachial Plexus Neuropathy, Hereditary .
Cervicobrachial Neuralgia .
Familial Brachial Plexus Neuritis .
Hereditary Brachial Plexus Neuropathy .
Hereditary Neuralgic Amyotrophy .
Heredofamilial Neuritis with Brachial Plexus Predilection .
Neuritis With Brachial Predilection .
Parsonage-Aldren-Turner Syndrome .
Shoulder Girdle Neuropathy .
Amyotrophic Neuralgias .
Amyotrophies, Hereditary Neuralgic .
Amyotrophies, Neuralgic .
Brachial Neuralgias .
Brachial Neuritides .
Brachial Plexus Neuritides .
Cervico Brachial Neuralgia .
Cervico-Brachial Neuralgias .
Cervicobrachial Neuralgias .
Girdle Neuropathies, Shoulder .
Girdle Neuropathy, Shoulder .
Hereditary Neuralgic Amyotrophies .
Neuralgia, Brachial .
Neuralgia, Cervico-Brachial .
Neuralgia, Cervicobrachial .
Neuralgias, Amyotrophic .
Neuralgias, Brachial .
Neuralgias, Cervico-Brachial .
Neuralgias, Cervicobrachial .
Neuralgic Amyotrophies .
Neuralgic Amyotrophies, Hereditary .
Neuralgic Amyotrophy, Hereditary .
Neuritides, Brachial .
Neuritides, Brachial Plexus .
Neuritis, Brachial .
Neuropathies, Shoulder Girdle .
Neuropathies, Shoulder-Girdle .
Neuropathy, Shoulder Girdle .
Neuropathy, Shoulder-Girdle .
Parsonage Aldren Turner Syndrome .
Parsonage Turner Syndrome .
Shoulder Girdle Neuropathies .
Shoulder-Girdle Neuropathies .
Syndrome, Parsonage-Aldren-Turner .
Syndrome, Parsonage-Turner .
Amyotrophy, Neuralgic .
Cervico-Brachial Neuralgia .
Neuralgia, Amyotrophic .
Neuralgic Amyotrophy .
Neuritis, Brachial Plexus .
Parsonage-Turner Syndrome .
Shoulder-Girdle Neuropathy .
BRACHIAL NEURALGIA .
A syndrome associated with inflammation of the BRACHIAL PLEXUS. Clinical features include severe pain in the shoulder region which may be accompanied by MUSCLE WEAKNESS and loss of sensation in the upper extremity. This condition may be associated with VIRUS DISEASES; IMMUNIZATION; SURGERY; heroin use (see HEROIN DEPENDENCE); and other conditions. The term brachial neuralgia generally refers to pain associated with brachial plexus injury. (From Adams et al., Principles of Neurology, 6th ed, pp1355-6) .
0.64
441244
 
Islet Amyloid Polypeptide .
Amlintide .
Amylin .
IAPP Precursor .
IAPP Protein .
Insulinoma Amyloid Polypeptide .
Insulinoma Amyloid Polypeptide Precursor .
Islet Amyloid Polypeptide Precursor .
Pancreatic Amylin .
Amylin, Pancreatic .
Amyloid Polypeptide, Insulinoma .
Amyloid Polypeptide, Islet .
Polypeptide, Insulinoma Amyloid .
Polypeptide, Islet Amyloid .
A pancreatic beta-cell hormone that is co-secreted with INSULIN. It displays an anorectic effect on nutrient metabolism by inhibiting gastric acid secretion, gastric emptying and postprandial GLUCAGON secretion. Islet amyloid polypeptide can fold into AMYLOID FIBRILS that have been found as a major constituent of pancreatic AMYLOID DEPOSITS. .
0.64
02179