Phenotypes for disease #05419 (RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis and skeletal dysplasia syndrome (RHYNS)), OMIM:602152)

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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000186693 - RHYNS see paper; ... Familial, autosomal recessive 38y - - - - Johan den Dunnen 00155014
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