Disease #02448 (CCM2 (cerebral cavernous malformations, type 2 (CCM-2)), OMIM:603284)

Official abbreviation CCM2
Name cerebral cavernous malformations, type 2 (CCM-2)
OMIM ID 603284
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene CCM2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00153314 - - - M - Taiwan - - - - - CCM2 - CCM2 CCM2 1 1 Kang-Yang Jih
00153315 - - - M no Taiwan - - - - - CCM2 - CCM2 CCM2 1 1 Kang-Yang Jih
00170858 34 - - F ? Italy - - - - - CCM2 Headache (HP:0002076), Cerebellar hemangiomas CCM2 CCM2 1 1 Carmela Fusco
00170859 35 - - M ? Italy - - - - - CCM2 Headache (HP:0002076), Epilepsy (HP:0001250), Fatigable weakness of skeletal (HP:0030197), Cerebellar hemangiomas, Bilateral lesions CCM2 CCM2 1 1 Carmela Fusco
00173728 42 - - M ? Italy - - - - - CCM2 Cerebellar hemangiomas CCM2 CCM2 1 1 Carmela Fusco
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