Phenotype #0000087044

Individual ID 00110289
Associated disease AT
Phenotype details affected male sibling with same mutations
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Frans BL Hogervorst
Database submission license No license selected
Created by Frans BL Hogervorst
Date created 2011-12-14 16:02:58 +01:00 (CET)
Date last edited 2015-12-18 21:01:32 +01:00 (CET)

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