Phenotype #0000000911

Individual ID 00001757
Associated disease SBCADD
Inheritance Unknown
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Onset -
Phenotype/Onset -
Phenotype details newborn screening; no clinical symptoms
Protein -
Age/Diagnosis -
Owner name Division of Human Genetics, Innsbruck
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Division of Human Genetics, Innsbruck
Date created 2010-07-30 12:56:48 +02:00 (CEST)
Date last edited 2013-03-27 15:14:02 +01:00 (CET)

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