" /> Dyssynergia cerebellaris myoclonica of hunt - CISMeF





Preferred Label : Dyssynergia cerebellaris myoclonica of hunt;

CISMeF acronym : CPD5;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Spinodentate atrophy; Myoclonus and ataxia; Cerebelloparenchymal disorder V; Ramsay hunt syndrome; CPD5;

Inheritance : Autosomal recessive;

Prefixed ID : 213400;

Details


You can consult :


Nous contacter.
30/04/2025


[Home] [Top]

© Rouen University Hospital. Any partial or total use of this material must mention the source.