RAP1GAP gene related symptoms and diseases
All the information presented here about the RAP1GAP gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to RAP1GAP gene
Symptoms // Phenotype | % Cases |
---|---|
Leukemia | Very Common - Between 80% and 100% cases |
Acute promyelocytic leukemia | Very Common - Between 80% and 100% cases |
Abnormal granulocytopoietic cell morphology | Very Common - Between 80% and 100% cases |
Rare diseases associated to RAP1GAP gene
Here you will find a list of rare diseases related to the RAP1GAP. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
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 RAP1GAP
Potential gene panels for RAP1GAP gene
RAP1GAP Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the RAP1GAP 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 NRXN3 COL18A1 RP9 KMT2B COL6A1 IARS2 SCN3A