Phenotype #0000001052

Individual ID 00002073
Associated disease SLOS
Inheritance Familial
Diagnosis/Initial -
Diagnosis/Definite -
Age/Onset -
Age/Examination -
Phenotype/Onset -
Phenotype details diagnosis fetal; ascertainment clinical presentation
Biochem -
Protein -
Severity_score -
Age/Diagnosis <00y00m00d
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 2011-04-20 16:34:50 +02:00 (CEST)
Date last edited 2012-10-02 12:59:22 +02:00 (CEST)

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