CD109 gene related symptoms and diseases

All the information presented here about the CD109 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to CD109 gene

Symptoms // Phenotype % Cases
Thrombocytopenia Very Common - Between 80% and 100% cases
Purpura Very Common - Between 80% and 100% cases
Petechiae Very Common - Between 80% and 100% cases
Neonatal alloimmune thrombocytopenia Very Common - Between 80% and 100% cases

Rare diseases associated to CD109 gene

Here you will find a list of rare diseases related to the CD109. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


FETAL AND NEONATAL ALLOIMMUNE THROMBOCYTOPENIA

Alternate names

FETAL AND NEONATAL ALLOIMMUNE THROMBOCYTOPENIA Is also known as nait

Description

Foetal/neonatal alloimmune thrombocytopaenia (NAIT) results from maternal alloimmunisation against foetal platelet antigens inherited from the father and different from those present in the mother, and usually presents as a severe isolated thrombocytopaenia in otherwise healthy newborns.

Most common symptoms of FETAL AND NEONATAL ALLOIMMUNE THROMBOCYTOPENIA

  • Thrombocytopenia
  • Purpura
  • Petechiae
  • Neonatal alloimmune thrombocytopenia


More info about FETAL AND NEONATAL ALLOIMMUNE THROMBOCYTOPENIA

SOURCES: ORPHANET


Potential gene panels for CD109 gene

Platelet Antigen Genotyping Panel Panel

United States.

By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti Platelet Antigen Genotyping Panel that also includes the following genes: CD109 GP1BA ITGA2 ITGA2B ITGB3

More info about this panel
United States.

CD109 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the CD109 gene.

More info about this panel
United States.

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ITGA7 TBL1XR1 CCNF ANKK1 KIF5A MLYCD EPM2A