Complement Component 9 Deficiency (C9D)

Alias:
C9 Deficiency
C9d
C9 Deficiency with Dermatomyositis
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Complement Component 9 Deficiency, also known as c9 deficiency, is related to complement deficiency and meningococcal meningitis. An important gene associated with Complement Component 9 Deficiency is C9 (Complement C9), and among its related pathways/superpathways are IL-9 Signaling Pathways and Spinal cord injury. Affiliated tissues include skeletal muscle, and related phenotypes are decreased circulating complement c9 concentration and Increased shRNA abundance (Z-score > 2)
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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3
30
16

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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