Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2 (CADASIL2)

Alias:

Htra1-Related Autosomal Dominant Cerebral Small Vessel Disease

Cadasil 2

Cadasil2

Autosomal Dominant Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Type 2

Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, 2

Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, Autosomal Dominant, 2

Htra1-Related Autosomal Dominant Cerebral Angiopathy

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2, also known as htra1-related autosomal dominant cerebral small vessel disease, is related to spondylosis and pseudobulbar palsy. An important gene associated with Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2 is HTRA1 (HtrA Serine Peptidase 1), and among its related pathways/superpathways are Collagen chain trimerization and Extracellular matrix organization. Affiliated tissues include brain, and related phenotypes are hyperintensity of cerebral white matter on mri and lacunar stroke

Related ID：

MALACARDS：CRB170

OMIM：616779

MESH：D046589