Any Moyamoya disease in which the cause of the disease is a mutation in the ACTA2 gene.
Comprehensive, easy-to-understand information about this condition
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moyamoya disease 1
MONDO:0009649
moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome
MONDO:0010448
Moyamoya disease 2
MONDO:0011784
moyamoya disease 3
MONDO:0012122
aortic aneurysm, familial thoracic 6
MONDO:0012730
Moyamoya disease with early-onset achalasia
MONDO:0014331