Disease #04016 (VRJS (Verheij syndrome (chromosome deletion syndrome 8q24.3)), OMIM:615583)

Official abbreviation VRJS
Name Verheij syndrome (chromosome deletion syndrome 8q24.3)
OMIM ID 615583
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 11
Phenotype entries for this disease 10
Associated with 1 gene PUF60
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-02-23 15:08:27 +01:00 (CET)


Individuals

11 entries on 1 page. Showing entries 1 - 11.
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00073735 - - - F no France - - - 3y - VRJS - - PUF60 1 1 Paul Kuentz
00073736 - - - M no - - - - 14y - VRJS - - PUF60 1 1 Paul Kuentz
00073737 - - - M no - - - - 7y - VRJS - - PUF60 1 1 Paul Kuentz
00073738 - - - M no Czech Republic - - - 17y - VRJS - - PUF60 1 1 Paul Kuentz
00073739 - - - F no Belgium - - - - - VRJS - - PUF60 1 1 Paul Kuentz
00078890 - - - F - - - - - - - VRJS - - PUF60 1 1 Paul Kuentz
00092262 - PubMed: Tarailo-Graovac 2016, Journal: Tarailo-Graovac 2016 - - - United States - - - - - PLCA1, VRJS facial dysmorphism, short stature (Verheij syndrome), mild IDD ,severe early onset eczema (amyloidosis, primary localized cutaneous, recessive) OSMR, PUF60 - - 1 Johan den Dunnen
00326212 173715 - prenatal sample - ultrasound abnormalities M ? Germany - - - - - VRJS (+) Abnormality of prenatal development or birth,(+) Increased nuchal translucency,(+) Fetal ultrasound soft marker,(+) Abnormal heart morphology PUF60 PUF60 1 1 Andreas Laner
00398755 - - - M - - - - - - - VRJS Verheij Syndrome - PUF60 1 1 Michael Hildebrand
00401513 127P - - F no Spain - - - - - ID, VRJS - - PUF60 1 1 Alejandro Brea-Fernández
00446741 281422 - - F no Germany - - - - - VRJS Neurodevelopmental delay, Delayed speech and language development, Poor fine motor coordination, Seizure, Generalized non-motor (absence) seizure, Generalized myoclonic seizure, Renal duplication, Abnormal finger phalanx morphology PUF60 PUF60 1 1 Andreas Laner
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