Afibrinogenemia, Congenital (CAFBN)

Alias:
Congenital Afibrinogenemia
Afibrinogenemia
Factor I Deficiency
Complement Factor I Deficiency
Hypofibrinogenemia, Congenital
Congenital Hypofibrinogenemia
Familial Afibrinogenemia
Fibrinogen Deficiency
Hypofibrinogenemia
Cafbn
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Afibrinogenemia, Congenital, also known as congenital afibrinogenemia, is related to familial afibrinogenemia and dysfibrinogenemia, congenital. An important gene associated with Afibrinogenemia, Congenital is FGG (Fibrinogen Gamma Chain), and among its related pathways/superpathways are Infectious disease and Metabolism of proteins. The drugs Protamines and Liver Extracts have been mentioned in the context of this disorder. Affiliated tissues include spleen and tongue, and related phenotypes are homeostasis/metabolism and nervous system
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
--
26
189
34

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!
Wechat
Comparison
Al agent
Tutorials
Back to top