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cadasil syndrome

Medical Definition

A hereditary cerebrovascular disorder caused by mutations in the notch 3 gene. it is characterized by alterations of the muscular wall of the small vessels in the brain, resulting in transient ischemic attacks. it may lead to cognitive problems and dementia.
Related Codes (1)
Code
Description
Billable
Details
I67.850Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

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