Phenotype #0000000581

Individual ID 00001149
Associated disease GA1
Inheritance Familial, autosomal recessive
Age/Onset 00y00m00d
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis -
Phenotype/Onset -
Phenotype details slowly developing psychomotor delay, hypotonia, dystonic postures, lethargy, macrocephaly, dystonia, was able to walk without help
Protein -
Biochem 3-OH-GA(urine): 215 mmol/mol creatinine (c: 2-14); GA(urine): 12271 mmol/mol creatinine (c: 2-10)
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 2013-11-20 14:31:59 +01:00 (CET)

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