Log In|Sign Up
ENCongenital Fibrinogen Deficiency
Alias:
Fibrinogen Deficiency, Congenital
Favorite
Congenital Fibrinogen Deficiency, also known as fibrinogen deficiency, congenital, is related to afibrinogenemia, congenital and rare hemorrhagic disorder. An important gene associated with Congenital Fibrinogen Deficiency is FGG (Fibrinogen Gamma Chain). Affiliated tissues include liver, and related phenotypes are fever and left ventricular hypertrophy
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
