Complement Factor I Deficiency (CFID)

Alias:
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
Related ID:
MESH:C572568
ICD11:1452989457

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
<1/1000000
6
44
13

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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