C10orf55 gene related symptoms and diseases

All the information presented here about the C10orf55 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to C10orf55 gene

Symptoms // Phenotype % Cases
Thrombocytopenia Very Common - Between 80% and 100% cases
Bruising susceptibility Very Common - Between 80% and 100% cases
Epistaxis Very Common - Between 80% and 100% cases
Menorrhagia Very Common - Between 80% and 100% cases
Joint hemorrhage Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with C10orf55 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Impaired epinephrine-induced platelet aggregation
  • Delayed onset bleeding
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Rare diseases associated to C10orf55 gene

Here you will find a list of rare diseases related to the C10orf55. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


QUEBEC PLATELET DISORDER


Alternate names

QUEBEC PLATELET DISORDER Is also known as bleeding disorder, platelet-type, 5, factor v quebec, bdplt5

Description

Quebec platelet syndrome (QPS) is a platelet granule disorder characterized by moderate to severe bleeding after trauma, surgery or obstetric interventions, frequent ecchymoses, mucocutaneous bleeding and muscle and joint bleeds.

Most common symptoms of QUEBEC PLATELET DISORDER

  • Thrombocytopenia
  • Bruising susceptibility
  • Epistaxis
  • Menorrhagia
  • Joint hemorrhage


More info about QUEBEC PLATELET DISORDER

SOURCES: ORPHANET OMIM MESH




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