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Summary Literature (0)
MIM:225790 - PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH

Xenbase Genes: flvcr2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009168 - Fowler syndrome

Disease Ontology (DO):
DOID:0111666 - proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome