hereditary cystatin C amyloid angiopathy (Q10992004)
Jump to navigation
Jump to search
a cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of CST3 on chromosome 20p11.21.
- CST3-related cerebral amyloid angiopathy
- Amyloidosis, Cerebroarterial, Icelandic Type
- Hereditary Cerebral Hemorrhage with Amyloidosis
- HCHWA
- Amyloidosis VI
- Cerebral Hemorrhage, Hereditary, with Amyloidosis
- Cystatin amyloidosis
- Hereditary cerebral hemorrhage with amyloidosis, Icelandic type
- Amyloidosis 6
- CEREBRAL AMYLOID ANGIOPATHY, CST3-RELATED
- HCHWA, Icelandic type
- CST3-related amyloidosis
- Hereditary cystatin C amyloid angiopathy
- Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant
- Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hereditary cystatin C amyloid angiopathy |
a cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of CST3 on chromosome 20p11.21. |
|
Statements
1 reference
1 reference
1 reference
.jpg)
437.8
1 reference
277.39
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference