Phenotype #0000010379

Individual ID 00011692
Associated disease GA1
Inheritance Familial, autosomal recessive
Age/Onset 00y11m
Diagnosis/Initial -
Age/Examination 01y00m (1 year)
Diagnosis/Definite -
Age/Diagnosis -
Phenotype/Onset -
Phenotype details regression, dystonia, seizure, athetosis, macrocephaly, MRI: basal nuclei malacia
Protein -
Biochem 3-OH-GA(urine): 58.56 (fold change vs. normal control); GA(urine): 359.07 (fold change vs. normal control)
Enzyme/Activity -
Owner name Svenja Wagner
Database submission license No license selected
Created by Svenja Wagner
Date created 2014-02-20 13:48:05 +01:00 (CET)
Date last edited 2014-04-28 13:36:26 +02:00 (CEST)

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