Annotation Detail
Information
- Associated Genes
- APOA1
- Associated Variants
-
APOA1 MUTATION
APOA1 MUTATION - Associated Disease
- Amyloid Neuropathies, Familial
- Source Database
- DisGeNET
- Description
- The single amino acid mutation G26R in human apolipoprotein A-I (apoA-I) is associated with familial amyloid polyneuropathy III.
- Pubmed
- 26292220
- Section of the abstract supporting the evidence
- ALL_TEXT_1/3
- Number of the section of the abstract supporting the evidence
- 1
- Number of the sentence supporting the evidence
- 1
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000542883744160607
Drugs