Phenotype #0000117398

Individual ID 00144662
Associated disease MRMV1
Phenotype details Clumsiness, difficulties in fine bimanual activities. Hands, forearms and arms. Gross motor development was slightly delayed.
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
MotorSkills -
Severity_score Woods & Teuber 2
Protein -
Brain/Imaging -
Owner name Tatjana Bierhals
Database submission license No license selected
Created by Tatjana Bierhals
Date created 2017-12-19 11:16:13 +01:00 (CET)
Date last edited 2018-02-27 03:36:50 +01:00 (CET)

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