01
Diseases
Amyloid Neuropathies, Familial
amyloid neuropathies, familial
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Amyloid Neuropathies, Familial
- Standard Disease Name
- amyloid neuropathies, familial
- MeSH Tree
- No data
- ICD-10
- E85.1
Identifiers
- DO ID
- No data
- MeSH ID
- D028227
- OMIM ID
- No data
- UMLS ID
- C0206245
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A rare inherited neuropathy characterized by deposition of amyloid in the peripheral nerves.|MSH2017_2016_08_12: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.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease8 Targets
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