Primary CD59 deficiency

Definition

Primary CD59 deficiency is a rare, genetic, hematologic and neurologic disease characterized by chronic, Coombs-negative hemolysis associated with early-onset, relapsing, immune-mediated, inflammatory, axonal or demyelinating, sensory-motor, peripheral polyneuropathy and isolated or recurrent cerebrovascular events (in anterior or posterior circulation).

Disease data

Classification

Disease

ORPHA code

169464

OMIM code

612300

ICD10 code

D84.1

ICD11 code

*Soruce