Phenotype #0000036698

Individual ID 00050080
Associated disease ACCPN
Phenotype details see paper; Andermann syndrome; hypotonia, areflexia lower extremities, reduced deep tendon reflexes iupper extremities with normal tonus, delayed motor milestones; MRI complete agenesis corpus callosum, disseminated white matter hyperintensities
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 07y (7 years)
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 2012-11-07 12:34:19 +01:00 (CET)
Date last edited 2015-09-19 21:47:01 +02:00 (CEST)

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