Phenotypes for disease #03789 (CDG1T (glycosylation, congenital disorder of, type It (CDG-1T)), OMIM:614921)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000170762 severe PGM1-CDG CDG CDG-1T Familial, autosomal recessive - - - birth - Silvia Radenkovic 00225659
0000170764 severe PGM1-CDG phenotype - CDG-1T Familial, autosomal recessive - - - birth - Silvia Radenkovic 00225660
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