Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000310319 Individual ID 00419032 Associated disease CCM Phenotype details epilepsy (HP:0001250); cerebellar hemangiomas Diagnosis/Initial cerebral cavernous malformations Inheritance Familial, autosomal dominant Diagnosis/Definite CCM1 Age/Examination 10y (10 years) Age/Diagnosis - Age/Onset 8y Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International 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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