Phenotype #0000310373

Individual ID 00419086
Associated disease CCM
Phenotype details intracranial hemorrhage; fatigable weakness skeletal muscles (HP:0030197); hemiparesis (HP:0001269); spinal hemangiomas
Diagnosis/Initial cerebral cavernous malformations
Inheritance Familial, autosomal dominant
Diagnosis/Definite CCM3
Age/Examination 23y (23 years)
Age/Diagnosis -
Age/Onset 18y
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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