Phenotype #0000210623

Individual ID 00275940
Associated disease MICPCH
Phenotype details pontocerebellar hypoplasia
Diagnosis/Initial -
Inheritance Familial, X-linked dominant
Diagnosis/Definite -
Age/Examination 12y (12 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Birth_Details -
Protein -
Owner name Enza Maria Valente
Database submission license No license selected
Created by Johan den Dunnen
Date created 2020-01-21 13:47:49 +01:00 (CET)
Date last edited 2020-01-24 15:00:09 +01:00 (CET)

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