Phenotype #0000128902

Individual ID 00163781
Associated disease MRMV1
Phenotype details delayed childhood motor milestones; 3y-head CT normal
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
MotorSkills Mild bilateral synkinesia
Severity_score -
Protein -
Brain/Imaging CT
Owner name Ashley Marsh
Database submission license No license selected
Created by Ashley Marsh
Date created 2018-04-12 04:08:04 +02:00 (CEST)
Date last edited 2020-01-10 12:28:57 +01:00 (CET)

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