Phenotypes for disease #00655 (BOR1 (branchiootorenal syndrome, with/without cataract, type 1 (BOR-1)), OMIM:113650)

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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     
0000129444 Hearing loss, fistulae, cleft palate, renal agenesis/hypoplasia - BOR1 Familial, autosomal dominant - - - - - Viviana Karina Dalamón 00164339
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