Phenotypes for disease #02732 (MCDR2 (dystrophy, macular, retinal, type 2 (MCDR2, Bull's eye macular dystrophy)), OMIM:608051)

3 entries on 1 page. Showing entries 1 - 3.
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     
0000026256 - - - Unknown - - - - - Pascal Escher 00032827
0000026258 - - - Unknown - - - - - Pascal Escher 00032829
0000275984 retinal dystrophy; MIM, 608051 MIM, 608051 - Familial, autosomal dominant - - - - - LOVD 00382142
Legend   How to query  


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