Phenotypes for disease #02932 (RCD3B (dystrophy, retinal cone, type 3B (RCD-3B)), OMIM:610356)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000127984 - CDSRR - Familial, autosomal recessive - - - - - Dror Sharon 00155484
0000127985 - CDSRR - Familial, autosomal recessive - - - - - Dror Sharon 00155485
0000127986 - CDSRR - Familial, autosomal recessive - - - - - Dror Sharon 00155486
0000127987 - CDSRR - Familial, autosomal recessive - - - - - Dror Sharon 00155487
0000127988 - CDSRR - Familial, autosomal recessive - - - - - Dror Sharon 00155488
0000127989 - CDSRR - Familial, autosomal recessive - - - - - Dror Sharon 00155489
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