| Metadata | |
|---|---|
| ID | DOID:0070027 |
| Name | CST3-related cerebral amyloid angiopathy |
| Definition | A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of the CST3 gene on chromosome 20p11.21. https://www.ncbi.nlm.nih.gov/pubmed/2900981 |
| Xrefs | |
| Synonyms |
Amyloidosis VI [EXACT] Amyloidosis, Cerebroarterial, Icelandic Type [EXACT] Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant [EXACT] HCHWA [EXACT] Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |