(Q10992004)
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.
- 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
Statements
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277.39
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Identifiers
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