CFD gene related symptoms and diseases

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

Top 5 symptoms and clinical features associated to CFD gene

Symptoms // Phenotype % Cases
Fever Very Common - Between 80% and 100% cases
Vomiting Very Common - Between 80% and 100% cases
Diarrhea Very Common - Between 80% and 100% cases
Recurrent infections Very Common - Between 80% and 100% cases
Respiratory tract infection Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with CFD gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Skin rash
  • Cough
  • Meningitis
  • Recurrent bacterial infections
  • Purpura
  • Shock
  • Complement deficiency
  • Recurrent bacterial meningitis

Rare diseases associated to CFD gene

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


RECURRENT NEISSERIA INFECTIONS DUE TO FACTOR D DEFICIENCY

Alternate names

RECURRENT NEISSERIA INFECTIONS DUE TO FACTOR D DEFICIENCY Is also known as factor d deficiency

Description

Recurrent Neisseria infections due to factor D deficiency is a rare, genetic, primary immunodeficiency disorder characterized by an increased susceptibility to Neisseria bacterial infections, resulting from complement factor D deficiency, typically manifesting as recurrent respiratory infections, recurrent meningitis and/or septicemia. Patients typically present fever, purpuric rash, arthralgia, myalgia and undetectable complement factor D plasma concentrations.

Most common symptoms of RECURRENT NEISSERIA INFECTIONS DUE TO FACTOR D DEFICIENCY

  • Fever
  • Vomiting
  • Diarrhea
  • Recurrent infections
  • Respiratory tract infection


More info about RECURRENT NEISSERIA INFECTIONS DUE TO FACTOR D DEFICIENCY

SOURCES: OMIM ORPHANET MESH


Potential gene panels for CFD gene

CFD Gene Sequencing Panel

United States.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center

This panel specifically test the CFD gene.

More info about this panel
United States.

CFD Deletion/duplication analysis Panel

United States.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center

This panel specifically test the CFD gene.

More info about this panel
United States.

Complement factor D deficiency Panel

Germany.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders

This panel specifically test the CFD gene.

More info about this panel
Germany.

Complement deficiencies Panel Panel

Germany.

By CeGaT GmbH Complement deficiencies Panel that also includes the following genes: CFB THBD SERPING1 C1QA C1QB C1QC C1R C1S C2 C3

More info about this panel
Germany.

CFD Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the CFD gene.

More info about this panel
United States.

Primary Immunodeficiency Panel Panel

Finland.

By Blueprint Genetics Primary Immunodeficiency Panel that also includes the following genes: RMRP RORC CFB BLM SH2D1A SLC7A7 SMARCAL1 SMARCD2 SRP72 BTK

More info about this panel
Finland.

Complement System Disorder Panel Panel

Finland.

By Blueprint Genetics Complement System Disorder Panel that also includes the following genes: CFB SPAG1 THBD SERPING1 RSPH1 C1QA C1QB C1QBP C1QC C1S

More info about this panel
Finland.

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