Phenotype #0000294299

Individual ID 00401280
Associated disease CCM
Phenotype details see paper; ...
Diagnosis/Initial multiple cerebral cavernous malformations
Inheritance Familial, autosomal dominant
Diagnosis/Definite CCM
Age/Examination -
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 2022-01-30 16:31:42 +01:00 (CET)
Date last edited N/A

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