Phenotypes for disease #02413 (USH1F (Usher syndrome, type 1F (USH-1F)), OMIM:602083)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000204967 - USH1 USH1F Familial, autosomal recessive - - - - - David Baux 00267037
0000305627 - - - Familial, autosomal recessive - - - - - Gemeinschaftspraxis für Humangenetik Dresden 00413662
0000350872 congenital bilateral hearing loss and first began to experience night blindness when the proband was about 10 years old USH USH1F Familial, autosomal recessive 26y 26y congenital congenital We Yanbao Xiang 00465320
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