ITGAL gene related symptoms and diseases
All the information presented here about the ITGAL gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to ITGAL gene
Symptoms // Phenotype | % Cases |
---|---|
Seizures | Uncommon - Between 30% and 50% cases |
Pericarditis | Uncommon - Between 30% and 50% cases |
Cerebral ischemia | Uncommon - Between 30% and 50% cases |
Myositis | Uncommon - Between 30% and 50% cases |
Raynaud phenomenon | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with ITGAL gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Gangrene
- Pulmonary infiltrates
- Pustule
- Uveitis
- Aseptic necrosis
- Pulmonary embolism
- Hemoptysis
- Keratoconjunctivitis sicca
And 97 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to ITGAL gene
Here you will find a list of rare diseases related to the ITGAL. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
BEHÇET DISEASE
Alternate names
BEHÇET DISEASE Is also known as bd, behcet disease
Description
Behçet's disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.
Most common symptoms of BEHÇET DISEASE
- Seizures
- Ataxia
- Neoplasm
- Pain
- Cataract
More info about BEHÇET DISEASE
ACUTE PROMYELOCYTIC LEUKEMIA
Alternate names
ACUTE PROMYELOCYTIC LEUKEMIA Is also known as acute myeloid leukemia with t(15;17)(q22;q12);(pml/raralpha) and variants, acute myeloblastic leukemia 3, apml, aml m3, aml with t(15;17)(q22;q12);(pml/raralpha) and variants, leukemia, acute promyelocytic
Description
Acute promyelocytic leukemia (APL) is an aggressive form of acute myeloid leukemia (AML; see this term), characterized by arrest of leukocyte differentiation at the promyelocyte stage, due to a specific chromosomal translocation t(15;17) in myeloid cells. APL manifests with easy bruising, hemorrhagic diathesis and fatigue.
Most common symptoms of ACUTE PROMYELOCYTIC LEUKEMIA
- Leukemia
- Acute promyelocytic leukemia
- Abnormal granulocytopoietic cell morphology
More info about ACUTE PROMYELOCYTIC LEUKEMIA
Search interest in ITGAL
Potential gene panels for ITGAL gene
Neutrophil Antigen Genotyping Panel (includes HNA-1, 3, 4, 5) Panel
By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti Neutrophil Antigen Genotyping Panel (includes HNA-1, 3, 4, 5) that also includes the following genes: SLC44A2 CD177 FCGR3B ITGAL ITGAM
More info about this panelITGAL Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the ITGAL gene.
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 PRRT2 UMOD HBB CTNS NCF2 MYLK2 TREX1