Phenotype #0000081292

Individual ID 00103215
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details see paper, epilepsy, hearing loss, developmental delay
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Sander Pajusalu
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Sander Pajusalu
Date created 2017-04-09 20:31:55 +02:00 (CEST)
Date last edited 2017-04-11 15:14:22 +02:00 (CEST)

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