Phenotype #0000157568

Individual ID 00208961
Associated disease EAOH
Phenotype details oculomotor apraxia, nystagmus (no further details given by physician)
Diagnosis/Initial Ataxia-ocular apraxia type 1
Inheritance Unknown
Diagnosis/Definite EAOH
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Rick van Minkelen