Phenotypes for disease #02478 (ADCADN (ataxia, cerebellar, deafness, and narcolepsy, autosomal dominant), OMIM:604121)

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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     
0000231199 Recurrent attacks of rotary vertigo, nausea, gait insecurity, partial tinnitus, no hearing loss, familial anamnesis Vestibular migraine, differential diagnosis: episodic ataxia type II; HPOs: Tinnitus, Nausea, Gait ataxia, Vertigo, Vestibular nystagmus - - Unknown 47y - - - - Andreas Laner 00305349
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