Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Amyloidosis, cerebroarterial, Britisch type

Cerebral amyloid angiopathy of the Britisch type is an autosomal dominant disorder with variable penetrance caused by a mutation of the ITM2B gene.

Systematic

Amyloidosis, cerebroarterial
Amyloidosis, cerebroarterial, Britisch type
ITM2B
Amyloidosis, cerebroarterial, Danish type
Amyloidosis, cerebroarterial, Dutch type
Amyloidosis, cerebroarterial, Icelandic type

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Orphanet article

Orphanet ID 316226 [^]
100.

OMIM.ORG article

Omim 176500 [^]
Update: April 29, 2019