Disease #00991 (Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome, OMIM:225790)

Official abbreviation -
Name Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome
OMIM ID 225790
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 9
Phenotype entries for this disease 0
Associated with 1 gene FLVCR2
Associated tissues -
Disease features -
Remarks -


Individuals

9 entries on 1 page. Showing entries 1 - 9.
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00247323 - PubMed: Lalonde 2010 - F - - - - 0 - - Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome - FLVCR2 FLVCR2 2 1 -
00247324 - PubMed: Meyer 2010 - M - - Pakistani - 0 - - Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome - FLVCR2 FLVCR2 2 1 -
00247325 - PubMed: Meyer 2010 - ? - - - - 0 - - Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome - FLVCR2 FLVCR2 2 1 -
00247326 - PubMed: Meyer 2010 - F - - Pakistani - 0 - - Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome - FLVCR2 FLVCR2 2 1 -
00247327 - PubMed: Meyer 2010 - F - - Pakistani - 0 - - Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome - FLVCR2 FLVCR2 2 1 -
00247328 - PubMed: Meyer 2010 Gender: M (phenotypically) M - - Pakistani - 0 - - Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome - FLVCR2 FLVCR2 2 1 -
00247329 - PubMed: Meyer 2010 - M - - Pakistani - 0 - - Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome - FLVCR2 FLVCR2 2 1 -
00247330 - PubMed: Meyer 2010 - M - - Pakistani - 0 - - Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome - FLVCR2 FLVCR2 2 1 -
00247331 - PubMed: Meyer 2010 - M - - Pakistani - 0 - - Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome - FLVCR2 FLVCR2 2 1 -
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