Phenotype #0000352879

Individual ID 00467713
Associated disease CCM
Phenotype details multiple abnormal signals frontotemporal/parietal lobes, brainstem, right basal ganglia, and right cerebellar hemisphere
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite CCM3
Age/Examination 07y (7 years)
Age/Diagnosis -
Age/Onset -
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 2025-10-27 19:36:21 +01:00 (CET)
Date last edited N/A

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