Phenotype #0000014898

Individual ID 00016306
Associated disease ID
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal recessive
Phenotype details cranio-lenticulo-sutural dysplasia (CLSD) and congenital disorders of glycosylation (CDG)-II
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Swati Gupta
Database submission license No license selected
Created by Swati Gupta
Date created 2014-03-05 20:59:04 +01:00 (CET)
Date last edited 2014-03-06 22:37:17 +01:00 (CET)

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