Phenotypes for disease #01517 (BSVD1;POREN1 (brain small vessel disease, type 1 (BSVD1);porencephaly, type 1 (POREN1)), OMIM:175780)

4 entries on 1 page. Showing entries 1 - 4.
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     
0000060548 Porencephaly 1 (OMIM:175780) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080979
0000275961 anterior segment developmental anomalies including glaucoma; MIM, 607595 MIM, 607595 - Familial, autosomal dominant - - - - - LOVD 00382119
0000285570 Abnormal vascular morphology, Abnormality of the vasculature - - Unknown 45y - - - - Andreas Laner 00392293
0000351461 bilateral cataracts microcornea porencephally - - Isolated (sporadic) - - - - - Javier Nogués - Castell 00466077
Legend   How to query  


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