F11-AS1 gene related symptoms and diseases

All the information presented here about the F11-AS1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.

Table of contents:

Main symptoms and clinical features
Other symptoms and clinical features
Related Diseases
Current trends

Top 5 symptoms and clinical features associated to F11-AS1 gene

Symptoms // Phenotype	% Cases
Bruising susceptibility	Very Common - Between 80% and 100% cases
Hematuria	Very Common - Between 80% and 100% cases
Abnormal bleeding	Very Common - Between 80% and 100% cases
Gastrointestinal hemorrhage	Very Common - Between 80% and 100% cases
Hepatitis	Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with F11-AS1 gene alterations may also develop some of the following symptoms and phenotypes:

Commonly - More than 50% cases
Epistaxis
Menorrhagia
Abnormal joint morphology
Prolonged partial thromboplastin time
Joint hemorrhage
Reduced factor XI activity
Chronic active hepatitis
Reduced factor VII activity

And 2 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to F11-AS1 gene

Here you will find a list of rare diseases related to the F11-AS1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.

CONGENITAL FACTOR XI DEFICIENCY

Alternate names

CONGENITAL FACTOR XI DEFICIENCY Is also known as f11 deficiency, plasma thromboplastin antecedent deficiency, hemophilia c, rosenthal syndrome, rosenthal factor deficiency, pta deficiency

Description

Congenital factor XI deficiency is an inherited bleeding disorder characterized by reduced levels and activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery.

Most common symptoms of CONGENITAL FACTOR XI DEFICIENCY

Bruising susceptibility
Hematuria
Abnormal bleeding
Gastrointestinal hemorrhage
Hepatitis

More info about CONGENITAL FACTOR XI DEFICIENCY

SOURCES: ORPHANET MESH OMIM

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