Phenotypes for disease #02723 (MCOPS6 (microphthalmia syndromic, type 6 (MCOPS-6)), OMIM:607932)

1 entry on 1 page. Showing entry 1.
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     
0000166899 mild delayed milestones, delayed speech, mild hypotonia, dysmorphic features, macrocephaly, post axial polydactyly - - - - - - - - Patrick R. Blackburn 00218415
Legend   How to query  


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