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

Official abbreviation ADCADN
Name ataxia, cerebellar, deafness, and narcolepsy, autosomal dominant
OMIM ID 604121
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene DNMT1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00305349 105298 - - F ? Germany - - - - - ADCADN 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 DSP DSP 1 1 Andreas Laner
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