HTRA1

HtrA serine peptidase 1
OMIM: 602194
PanelMode of inheritanceDetails
2 panels
R-numbers: R58
Signed-off version 2.178
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
dementia (disease), MONDO:0001627, CARASIL syndrome, OMIM:600142, Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2, OMIM:616779
R-numbers: R62
Signed-off version 1.25
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
CARASIL syndrome, 600142, Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2, 616779