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

10 entries on 1 page. Showing entries 1 - 10.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000053559 - - - Isolated (sporadic) - - - - - Paul Kuentz 00073735
0000053560 - - - Isolated (sporadic) - - - - - Paul Kuentz 00073736
0000053561 - - - Isolated (sporadic) - - - - - Paul Kuentz 00073737
0000053562 - - - Isolated (sporadic) - - - - - Paul Kuentz 00073739
0000053563 - - - Isolated (sporadic) - - - - - Paul Kuentz 00073738
0000058648 - - - Familial, autosomal dominant - - - - - Paul Kuentz 00078890
0000070598 facial dysmorphism, short stature (Verheij syndrome) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00092262
0000244673 (+) Abnormality of prenatal development or birth,(+) Increased nuchal translucency,(+) Fetal ultrasound soft marker,(+) Abnormal heart morphology - - Unknown 00y - - - - Andreas Laner 00326212
0000291839 Verheij Syndrome - - Isolated (sporadic) - - - - - Michael Hildebrand 00398755
0000335945 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 - - Isolated (sporadic) 06y - - - - Andreas Laner 00446741
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.