DiseaseID 6194

淀粉样神经病

disease

NCI2016_02D:Neuropathy caused by amyloid deposition in the peripheral nerves.|MSH2017_2016_08_12:Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (no

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Disease: 1Symptom: 12Target: 9Links: 21
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Record Fields

Scalar fields from the final disease record.

Disease Id
6194
Core Entity Id
62812
Source Entity Count
1
Preferred Name
Amyloid Neuropathies
Name Cn
淀粉样神经病
Name Pinyin
Dian Fen Yang Shen Jing Bing
Name En
Amyloid Neuropathies
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Nervous System Diseases; Nutritional and Metabolic Diseases
Do Class
Hpo Class
Mesh Class Name
Nutritional and Metabolic Diseases; Nervous System Diseases
Hpo Class Name
Do Class Name
Disease Definition
NCI2016_02D:Neuropathy caused by amyloid deposition in the peripheral nerves.|MSH2017_2016_08_12: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)
Version
v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Amyloid Neuropathies
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS004352
Me Sh
D017772
Umls
C0206247
Sym Map
SMDE05795
Dis Ge Net
C0206247
Umls Sty
T047
Me Sh Class
C10C18
Tcmbank Disease
13296

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_02D:Neuropathy caused by amyloid deposition in the peripheral nerves.|MSH2017_2016_08_12: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)
Me Sh Disease Class
Nervous System Diseases; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Nutritional and Metabolic Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome