All diseases

OMIM ID
225790
OMIM term:
PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH
Alternative terms:
HYDRANENCEPHALY, FOWLER TYPE
HYDROCEPHALY/HYDRANENCEPHALY DUE TO CEREBRAL VASCULOPATHY
ENCEPHALOCLASTIC PROLIFERATIVE VASCULOPATHY; EPV
(∗) Location:
14q24.3  
(†) Associated OMIM genes:
FLVCR2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/y23ipiox