Phenotype #0000188722

Individual ID 00249859
Associated disease CDG1K
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Bobby Ng
Database submission license No license selected
Created by Bobby Ng
Date created 2015-12-10 00:30:21 +01:00 (CET)
Date last edited N/A

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