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

Official abbreviation PVHH
Name Proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome
OMIM ID 225790
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 9
Phenotype entries for this disease -
Associated with 1 gene FLVCR2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

9 entries on 1 page. Showing entries 1 - 9.
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00247323 - PubMed: Lalonde 2010 - F - - - - - - - PVHH - FLVCR2 FLVCR2 2 1 LOVD
00247324 - PubMed: Meyer 2010 - M - - Pakistani - - - - PVHH - FLVCR2 FLVCR2 2 1 LOVD
00247325 - PubMed: Meyer 2010 - ? - - - - - - - PVHH - FLVCR2 FLVCR2 2 1 LOVD
00247326 - PubMed: Meyer 2010 - F - - Pakistani - - - - PVHH - FLVCR2 FLVCR2 2 1 LOVD
00247327 - PubMed: Meyer 2010 - F - - Pakistani - - - - PVHH - FLVCR2 FLVCR2 2 1 LOVD
00247328 - PubMed: Meyer 2010 Gender: M (phenotypically) M - - Pakistani - - - - PVHH - FLVCR2 FLVCR2 2 1 LOVD
00247329 - PubMed: Meyer 2010 - M - - Pakistani - - - - PVHH - FLVCR2 FLVCR2 2 1 LOVD
00247330 - PubMed: Meyer 2010 - M - - Pakistani - - - - PVHH - FLVCR2 FLVCR2 2 1 LOVD
00247331 - PubMed: Meyer 2010 - M - - Pakistani - - - - PVHH - FLVCR2 FLVCR2 2 1 LOVD
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