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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Amyloid Neuropathies, Familial [Disease/Finding] | |
| Synonyms |
Hereditary Neuropathic Amyloidosis Amyloid Neuropathies, Familial Familial Amyloid Polyneuropathies |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000010997 |
|
| altLabel |
Hereditary Neuropathic Amyloidosis Amyloid Neuropathies, Familial Familial Amyloid Polyneuropathies
|
|
| cui |
C0206245
|
|
| MESH DEFINITION |
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.
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|
| MESH DUI |
D028227
|
|
| MeSH name |
Amyloid Neuropathies, Familial
|
|
| MESH UI |
M0026861
|
|
| NDFRT kind |
DISEASE_KIND
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|
| notation |
N0000010997
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|
| NUI |
N0000010997
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|
| prefLabel |
Amyloid Neuropathies, Familial [Disease/Finding]
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|
| SNOMED CID |
42295001
|
|
| tui |
T047
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|
| subClassOf |
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