Disease #02449 (CCM3 (cerebral cavernous malformations, type 3 (CCM-3)), OMIM:603285)

Official abbreviation CCM3
Name cerebral cavernous malformations, type 3 (CCM-3)
OMIM ID 603285
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene PDCD10
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.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00153316 - - - M no Taiwan - - - - - CCM3 - PDCD10 PDCD10 1 1 Kang-Yang Jih
00170860 36 - - F ? Italy - - - - - CCM3 Intracranial haemorrhage, fatigable weakness of skeletal, Hemiparesis (HP:0001269), Sovratentorial hemangiomas PDCD10 PDCD10 1 1 Carmela Fusco
00170861 38 - - M ? Italy - - - - - CCM3 Behavioural psychiatric abnormalities (HP:0000708), Cerebellar hemangiomas PDCD10 PDCD10 1 1 Carmela Fusco
00170862 39 - - M ? Italy - - - - - CCM3 Behavioural psychiatric abnormalities (HP:0000708) PDCD10 PDCD10 1 1 Carmela Fusco
00170863 40 - - F - Italy - - - - - CCM3 Headache (HP:0002076), Behavioural psychiatric abnormalities (HP:0000708), Sovratentorial hemangiomas PDCD10 PDCD10 1 1 Carmela Fusco
Legend   How to query  


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