Phenotype #0000000919

Individual ID 00001765
Associated disease SBCADD
Inheritance Familial
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Onset -
Phenotype/Onset -
Phenotype details family analysis; 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 2013-04-26 13:31:41 +02:00 (CEST)
Date last edited 2013-05-13 09:32:02 +02:00 (CEST)

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