Phenotypes for disease #00462 (CDA (dystrophy, cornea, Avellino type (CDA)), OMIM:607541)

8 entries on 1 page. Showing entries 1 - 8.
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     
0000017116 CDA - - Unknown - - - - - Daniel Schorderet 00019126
0000017120 CDA - - Unknown - - - - - Daniel Schorderet 00019130
0000017121 CDA (resseembling SVGD) - - Unknown - - - - - Daniel Schorderet 00019131
0000017123 CDA (type II corneal opacity: reticular) - - Unknown - - - - - Daniel Schorderet 00019133
0000017124 CDL+CDA - - Unknown - - - - - Daniel Schorderet 00019134
0000017125 CDA (with no lattice-type deposition observed) - - Unknown - - - - - Daniel Schorderet 00019135
0000017166 CDA - - Unknown - - - - - Daniel Schorderet 00019172
0000053483 LVEF 0.36, skeletal myopathy (HP:0003756), implantable cardioverter-defibrillator - - Familial - 19y - - - Johan den Dunnen 00073732
Legend   How to query  


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