Phenotypes for disease #03782 (SANDD (dysfunction, node, sinoatrial and deafness (SANDD)), OMIM:614896)

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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     
0000078819 see paper; ..., congenital deafness, bradycardia - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100608
0000078820 see paper; ..., congenital deafness, bradycardia - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100607
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