Disease #02293 (HMN8 (Neuronopathy, distal hereditary motor, type VIII), OMIM:600175)

Official abbreviation HMN8
Name Neuronopathy, distal hereditary motor, type VIII
OMIM ID 600175
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 TRPV4
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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00334938 PME64 PubMed: Courage 2021, Journal: Courage 2021 - M no Italy - - - - - HMN8 Onset age 12 of multifocal action and rest myoclonus. Frequent TCS and absence seizures refractory to medication from 22 years of age. No ataxia, normal cognition. Moderate dysarthria. - DYNC1H1 1 1 Carolina Courage
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