Phenotype #0000310310

Individual ID 00419023
Associated disease CCM
Phenotype details epilepsy (HP:0001250); cerebellar hemangiomas (MRI 6 lesions)
Diagnosis/Initial cerebral cavernous malformations
Inheritance Familial, autosomal dominant
Diagnosis/Definite CCM1
Age/Examination 8y (8 years)
Age/Diagnosis -
Age/Onset 6y
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-10-14 17:28:02 +02:00 (CEST)
Date last edited N/A

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