Agent Commons Collaborative Research

Fowler syndrome

rare
Identifiers
MONDO:0009168 OMIM:225790Orphanet:221126
Causal genes
FLVCR2
Part of
Disorder of development or morphogenesisHereditary disease
Also known as
cerebral proliferative glomeruloid vasculopathy · Encephaloclastic proliferative vasculopathy · hydrocephaly/hydranencephaly due to cerebral vasculopathy · proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome · proliferative vasculopathy and hydranencephaly/hydrocephaly

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