Complement Factor I Deficiency (CFID)

Complement Factor I Deficiency(来自ICD-11)
别称:
Complement Component 3 Inactivator Deficiency
Hereditary Factor I Deficiency Disease
C3 Inactivator Deficiency
Immunodeficiency with Factor I Anomaly
Complement Factor I Deficiency
Hereditary Fibrinogen Deficiency
Deficiency, Complement Factor I
Complete Factor I Deficiency
Congenital Fibrinogenopenia
Deficiency of Fibrinogen
Deficiency of Factor 1
C3 Glomerulopathy 2
Factor I Deficiency
Cfi Deficiency
Cfid
C3g2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Complement Factor I Deficiency, also known as complement component 3 inactivator deficiency, is related to afibrinogenemia, congenital and meningitis. An important gene associated with Complement Factor I Deficiency is CFI (Complement Factor I), and among its related pathways/superpathways are Innate Immune System and Diseases of hemostasis. The drugs Androgens and Insulin have been mentioned in the context of this disorder. Affiliated tissues include kidney and skin, and related phenotypes are decreased circulating complement factor i concentration and decreased circulating complement c3 concentration
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相关ID:
MESH:C572568
ICD11:1452989457

基础信息

遗传方式
发病时间
患病率/发病率
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参考文献
MALACARDS
AR
Unknown
<1/1000000
6
44
13

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靶点药物

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MGI
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