Phenotype #0000060658

Individual ID 00081089
Associated disease CDG-1D
Phenotype details Congenital disorder of glycosylation, type Id (OMIM:601110)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Daniel Trujillano