Phenotype #0000252703

Individual ID 00334955
Associated disease Apert
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite Apert Syndrome
Age/Examination -
Age/Diagnosis 00y06m
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Malak Alghamdi
Database submission license No license selected
Created by Malak Alghamdi
Date created 2021-03-02 15:28:09 +01:00 (CET)
Date last edited 2021-03-03 09:17:28 +01:00 (CET)

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