Disease #01183 (BAVM (arteriovenous malformation, cerebral, brain (BAVM), OMIM:108010)

Official abbreviation BAVM
Name arteriovenous malformation, cerebral, brain (BAVM
OMIM ID 108010
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 2 genes IL6, KRAS
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Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-01-11 15:49:56 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00170852 30 paper submitted - F ? Italy - 19y - - - BAVM Intracranial haemorrage,Cerebellar hemangiomas, bilateral lesion KRIT1 KRIT1 1 1 Carmela Fusco
00398662 patient PubMed: Walcott 2018 - F ? (United Kingdom (Great Britain)) White - - - surgery BAVM cerebral hemorrhage (HP:0001342), recurrent brain arteriovenous malformations - CEP72, FAM109B, FBXO7, HPGD, ITGAX, MFNG, OPRM1, OR1N1, SMAD9 9 1 Litika Vermani
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