Phenotypes for disease #02140 (CSNB2A (blindness, night, stationary, congenital, type 2A (CSNB-2A)), OMIM:300071)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000275980 retinal dystrophy; MIM, 300071, 300600, or 300476 MIM, 300071, 300600, or 300476 - Familial, X-linked - - - - - LOVD 00382138
0000275982 retinal dystrophy; MIM, 300071, 300600, or 300476 MIM, 300071, 300600, or 300476 - Familial, X-linked - - - - - LOVD 00382140
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