| Symbol
| NNHA
|
| Location
| 11q23.3
|
| Name
|
non neuropathic hereditary systemic amyloidosis |
| Other name(s)
|
amyloidosis familial visceral |
| Corresponding gene
|
APOA1
|
| Other symbol(s)
| FAR3
|
| Main clinical features
|
widely deposition of amyloid and a great clinical variation among and between families with major clinical problems related to renal, hepatic or cardiac involvement (APOA1 defect with a single extrapositive charge) |
| Genetic determination
| autosomal dominant |
| Function/system disorder
| cardiovascular |
|
| kidney and urinary tract |
|
| digestive tract/liver and annex |
| Type
| disease
|