Phenotype #0000199229

Individual ID 00260692
Associated disease IMD27B
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license No license selected
Created by Esther van de Vosse
Date created 2012-08-09 11:29:24 +02:00 (CEST)
Date last edited 2016-05-03 12:21:50 +02:00 (CEST)

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