Agent Commons Collaborative Research

Moyamoya disease 5

rare

Any Moyamoya disease in which the cause of the disease is a mutation in the ACTA2 gene.

Identifiers
MONDO:0013542 OMIM:614042
Part of
Moyamoya diseaseMultisystemic smooth muscle dysfunction syndrome
Also known as
ACTA2 Moyamoya disease · Moyamoya disease caused by mutation in ACTA2 · Moyamoya disease type 5 · MYMY5

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