All diseases

OMIM ID
607595
OMIM term:
BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE
Alternative terms:
INFANTILE HEMIPARESIS
RETINAL ARTERIOLAR TORTUOSITY, INFANTILE HEMIPARESIS, AND LEUKOENCEPHALOPATHY, AUTOSOMAL DOMINANT BRAIN SMALL VESSEL DISEASE WITH AXENFELD-RIEGER ANOMALY, INCLUDED
LEUKOENCEPHALOPATHY WITH AXENFELD-RIEGER ANOMALY, INCLUDED
(∗) Location:
13q34  
(†) Associated OMIM genes:
COL4A1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/bue0hims