CR1 gene related symptoms and diseases
All the information presented here about the CR1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to CR1 gene
Symptoms // Phenotype | % Cases |
---|---|
Cognitive impairment | Uncommon - Between 30% and 50% cases |
Anemia | Uncommon - Between 30% and 50% cases |
Fever | Uncommon - Between 30% and 50% cases |
Respiratory distress | Uncommon - Between 30% and 50% cases |
Headache | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with CR1 gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Thrombocytopenia
- Myalgia
- Retinopathy
- Nausea and vomiting
- Hyperbilirubinemia
- Abnormality of blood and blood-forming tissues
- Acute kidney injury
- Reduced consciousness/confusion
And 3 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to CR1 gene
Here you will find a list of rare diseases related to the CR1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
MALARIA
Description
Malaria is a preventable life-threatening parasitic disease caused by Plasmodium (P. ) parasites that are transmitted by Anophles mosquito bites to humans and is typically clinically characterized by attacks of fever, headache, chills and vomiting.
Most common symptoms of MALARIA
- Cognitive impairment
- Anemia
- Fever
- Respiratory distress
- Headache
More info about MALARIA
KNOPS BLOOD GROUP SYSTEM; KN
Search interest in CR1
Potential gene panels for CR1 gene
AllNeuro panel Panel
By Centogene AG - the Rare Disease Company AllNeuro panel that also includes the following genes: BCS1L ROR2 RPL10 BDNF RPS6KA3 RTN2 RYR1 SACS BIN1 SBF1
More info about this panelAlzheimer: MAPT, CLU, PICALM, CR1 genes screening Panel
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Alzheimer: MAPT, CLU, PICALM, CR1 genes screening that also includes the following genes: PICALM CLU CR1 MAPT
More info about this panelCR1 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the CR1 gene.
More info about this panelATYPICAL HEMOLYTIC UREMIC SYNDROME: NGS PANEL Panel
By Laboratorio de Genetica Clinica SL ATYPICAL HEMOLYTIC UREMIC SYNDROME: NGS PANEL that also includes the following genes: CFB THBD C1S C2 C3 C3AR1 C8A C9 CFHR4 CFHR3
More info about this panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NDUFV1 CCND2 PAM16 MTMR2 MLYCD CIC WNT1