Phenotype #0000000382

Individual ID 00000950
Associated disease GA1
Inheritance Familial, autosomal recessive
Age/Onset -
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis -
Phenotype/Onset -
Phenotype details At age 09y: Motor dyspraxia, learning difficulties; CT: frontotemporal atrophy
Protein -
Biochem GA(urine) & 3-OH-GA(urine): excessively increased; carnitine(serum): marked deficiency
Enzyme/Activity -
Owner name Katrin Hinderhofer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2013-04-17 17:21:21 +02:00 (CEST)
Date last edited 2019-02-25 13:00:23 +01:00 (CET)

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