Phenotype #0000087491

Individual ID 00111406
Associated disease DEE7
Phenotype details Developmental delay, hypotonia, seizures during first year of life
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Bernt Popp
Database submission license No license selected
Created by Bernt Popp
Date created 2017-08-03 07:27:06 +02:00 (CEST)
Date last edited 2017-08-04 09:29:30 +02:00 (CEST)

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