Phenotypes for disease #00523 (renal failure (renal failure))

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     
0000017606 nephrotic syndrome, renal biopsy, revealing renal amyloidosis (IHC excluded AA type ); echocardiogram, electromyogram and liver examination ruled out extra-renal involvement - - Familial, autosomal dominant 42y - - - - Johan den Dunnen 00019882
0000017608 proteinuria; renal biopsy revealed amyloid deposition glomeruli - - Isolated (sporadic) 46y - - - - Johan den Dunnen 00019884
0000017609 34y-progressive renal dysfunction; 56y-amyloidosis on renal; echocardiogram showed mild intraventricular propeptides - - Familial 56y - - - - Johan den Dunnen 00019885
0000350777 HP:0000089, HP:0000104, HP.0008678, HP:0010958, HP:0012584, HP:0012582, HP:0001627, HP:0001638, HP:0011723, HP:0045017, HP:0002089 multiple congenital abnormalities, renal agenesis RHDA3 Familial, autosomal dominant - - - - - Marketa Wayhelova 00465242
Legend   How to query  


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.