Phenotype #0000167954

Individual ID 00222752
Associated disease IBGC1
Phenotype details brain calcifications
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Wanjin Chen
Database submission license No license selected
Created by Wanjin Chen
Date created 2019-02-11 11:05:07 +01:00 (CET)
Date last edited 2019-02-11 13:18:02 +01:00 (CET)

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