All individuals with variants in gene PTCHD2

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00390029 16 PubMed: Ruberto 2020 - ? - Italy - - - - - retinal disease Very pale optic disk, chorioretinal atrophy in macular area, highly altered fundus 1 1 LOVD
00412359 Fam3 PubMed: Halvardson 2016 - M - Sweden - - - - - NDD global developmental dealy, infantile spasms, hypsarrhythmia, bilateral multifocal epileptiform discharges, generalized tonic-clinic seizures, absent speech, hypotonia, inability to walk, hyperopia, astigmatism, thin corpus callosum, diffuse white matter abnormalities 1 1 Johan den Dunnen
Legend   How to query  


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