Disease #04016

Official abbreviation VRJS
Name Verheij syndrome (VRJS)
OMIM ID 615583
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene PUF60
Associated tissues -
Disease features -
Remarks -


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00073735 - - - F no France - - 0 3y - VRJS - - PUF60 1 1 Paul Kuentz
00073736 - - - M no - - - 0 14y - VRJS - - PUF60 1 1 Paul Kuentz
00073737 - - - M no - - - 0 7y - VRJS - - PUF60 1 1 Paul Kuentz
00073738 - - - M no Czech Republic - - 0 17y - VRJS - - PUF60 1 1 Paul Kuentz
00073739 - - - F no Belgium - - 0 - - VRJS - - PUF60 1 1 Paul Kuentz
00078890 - - - F - - - - 0 - - VRJS - - PUF60 1 1 Paul Kuentz
00092262 - PubMed: Tarailo-Graovac 2016, Journal: Tarailo-Graovac 2016 - - - United States - - 0 - - VRJS, amyloidosis, cutaneous facial dysmorphism, short stature (Verheij syndrome), mild IDD ,severe early onset eczema (amyloidosis, primary localized cutaneous, recessive) OSMR, PUF60 - 0 1 Johan den Dunnen
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