Phenotype #0000020186

Individual ID 00022415
Associated disease MRT
Phenotype details mild intellectual disability and epilepsy; no signs of myopathy
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination >26y (later than 26 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Arnaud Vanlander
Database submission license No license selected
Created by Johan den Dunnen
Date created 2014-10-11 12:23:37 +02:00 (CEST)
Date last edited N/A

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