FNDC3B gene related symptoms and diseases

All the information presented here about the FNDC3B 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.

Table of contents:

Main symptoms and clinical features
Related Diseases
Current trends
Suitable testing panels

Top 5 symptoms and clinical features associated to FNDC3B 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 FNDC3B gene

Here you will find a list of rare diseases related to the FNDC3B. 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.