Phenotypes for disease #03938 (MYP22 (myopia, autosomal dominant, type 22 (MYP-22)), OMIM:615420)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Eye/Cornea     

Protein     

Owner     

Individual ID     
0000021578 see paper; cataract, refractive error -20.00 diopteries, axial length (R=33.7/L=33.5) - - Familial, autosomal dominant - - - - myopia severe - Johan den Dunnen 00025465
0000021579 see paper; refractive index -2.50 to -11.0 dipteries (6/7 severe), extended axial length - - Familial, autosomal dominant - - - - myopia - Johan den Dunnen 00025466
0000021580 - - - Unknown - - - - myopia - Johan den Dunnen 00025467
0000021581 see paper - - Isolated (sporadic) - - - - myopia severe - Johan den Dunnen 00025468
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