Phenotype #0000093255

Individual ID 00117867
Associated disease CDG1P
Phenotype details unremarkable prenatal and neonatal period, hypotonia, hypertonia, developmental delay, mental retardation, epilepsy, strabismus convergens
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Christian Thiel
Database submission license No license selected
Created by Christian Thiel
Date created 2011-11-09 12:17:38 +01:00 (CET)
Date last edited 2011-11-11 14:58:41 +01:00 (CET)

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