Phenotype #0000222979

Individual ID 00289361
Associated disease CCM1
Diagnosis/Initial cerebral cavernous malformations, type 1 (CCM-1)
Diagnosis/Definite cerebral cavernous malformations, type 1 (CCM-1)
Phenotype details HP:0001250, HP:0007359
Inheritance Familial, autosomal dominant
Age/Examination 20y (20 years)
Age/Diagnosis 20y
Age/Onset 08y
Phenotype/Onset HP:0001250
Protein -
Owner name Stefania Battistini
Database submission license No license selected
Created by Stefania Battistini
Date created 2020-03-05 13:22:45 +01:00 (CET)
Date last edited 2020-04-02 19:59:35 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.