Phenotype #0000283616

Individual ID 00390078
Associated disease MRMV
Phenotype details moderate global delay; special education; OFC -0.5 SD; no epilepsy; gait ataxia, severe dyspraxia; dystonia lower limb
Diagnosis/Initial congenital mirror movement
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 8y6m (8 years, 6 months)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-11-09 17:45:02 +01:00 (CET)
Date last edited N/A

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