hereditary cystatin C amyloid angiopathy
a cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of CST3 on chromosome 20p11.21.
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hereditary cystatin C amyloid angiopathy
Summary
hereditary cystatin C amyloid angiopathy is a rare disease[1].
Key Facts
- hereditary cystatin C amyloid angiopathy's instance of is recorded as rare disease[2].
- hereditary cystatin C amyloid angiopathy's instance of is recorded as class of disease[3].
- hereditary cystatin C amyloid angiopathy is a type of cerebral amyloid angiopathy[4].
- hereditary cystatin C amyloid angiopathy is a type of genetic disease[5].
- hereditary cystatin C amyloid angiopathy is a type of autosomal dominant disease[6].
- hereditary cystatin C amyloid angiopathy's ICD-9-CM is recorded as 437.8[7].
- hereditary cystatin C amyloid angiopathy's ICD-9-CM is recorded as 277.39[8].
- hereditary cystatin C amyloid angiopathy's genetic association is recorded as CST3[9].
- hereditary cystatin C amyloid angiopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070027[10].
- hereditary cystatin C amyloid angiopathy's exact match is recorded as http://identifiers.org/doid/DOID:0070027[11].
- hereditary cystatin C amyloid angiopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_100008[12].
- hereditary cystatin C amyloid angiopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].