Phenotype #0000070588

Individual ID 00092254
Associated disease RTT
Inheritance Familial, X-linked dominant
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Phenotype details ID, epilepsy, autism, ataxia, developmental regression, cerebral folate deficiency (Rett Syndrome)
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 2016-12-16 19:09:22 +01:00 (CET)
Date last edited N/A

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