Phenotypes for disease #03680 (CSNB1E (blindness, night, stationary, congenital, type 1E (CSNB1E)), OMIM:614565)

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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     
0000067568 - - - Familial, autosomal recessive - 11 0d - - Soumittra Nagasamy 00088061
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