Phenotype #0000157588

Individual ID 00208981
Associated disease EAOH
Phenotype details see paper; ...
Diagnosis/Initial early onset cerebellar ataxia associated with oculomotor apraxia
Inheritance Familial, autosomal recessive
Diagnosis/Definite EAOH
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen