ZBTB16 gene related symptoms and diseases
All the information presented here about the ZBTB16 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,ORPHANET,HGNC,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to ZBTB16 gene
Symptoms // Phenotype | % Cases |
---|---|
Neoplasm | Rare - less than 30% cases |
Delayed skeletal maturation | Rare - less than 30% cases |
Beta-cell dysfunction | Rare - less than 30% cases |
Leukemia | Rare - less than 30% cases |
Acute promyelocytic leukemia | Rare - less than 30% cases |
Other less frequent symptoms and clinical features
Patients with ZBTB16 gene alterations may also develop some of the following symptoms and phenotypes:Rarely - Less than 30% cases
- Abnormal granulocytopoietic cell morphology
- Intellectual disability
- Short stature
- Microcephaly
- Strabismus
- Abnormal facial shape
- Cryptorchidism
- Intellectual disability, severe
And 44 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to ZBTB16 gene
Here you will find a list of rare diseases related to the ZBTB16. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
POLYCYSTIC OVARY SYNDROME 1; PCOS1
Alternate names
POLYCYSTIC OVARY SYNDROME 1; PCOS1 Is also known as pco, pco1, hyperandrogenemia, stein-leventhal syndrome, pcos
Description
a health problem that can affect a woman's menstrual cycle, fertility, hormones, insulin production, heart, blood vessels, and appearance
Most common symptoms of POLYCYSTIC OVARY SYNDROME 1; PCOS1
- Neoplasm
- Abnormality of metabolism/homeostasis
- Obesity
- Diabetes mellitus
- Apnea
More info about POLYCYSTIC OVARY SYNDROME 1; PCOS1
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
SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION
Most common symptoms of SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION
- Intellectual disability
- Short stature
- Microcephaly
- Strabismus
- Abnormal facial shape
More info about SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION
PRECURSOR T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA
Alternate names
PRECURSOR T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA Is also known as precursor t-cell acute lymphoblastic leukemia/lymphoma, t-all, precursor t-cell acute lymphocytic leukemia, precursor t-cell acute lymphocytic leukemia/lymphoma
More info about PRECURSOR T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA
SOURCES: ORPHANET
Search interest in ZBTB16
Potential gene panels for ZBTB16 gene
RT-PCR t(11;17) Panel
By CGC Genetics RT-PCR t(11;17) that also includes the following genes: ZBTB16 RARA
More info about this panelAllNeuro 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 panelIntellectual Disability NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Intellectual Disability NGS Panel that also includes the following genes: BCS1L RPS6KA3 SACS BIN1 SCN1A SCN8A SDCCAG8 SGCA SGSH ST3GAL3
More info about this panelZBTB16 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the ZBTB16 gene.
More info about this panelCaris MI TumorSeek 592-Gene NGS Panel Panel
By Caris Life Sciences Caris MI TumorSeek 592-Gene NGS Panel that also includes the following genes: BCL6 BCL7A BCL9 BCR ROS1 RPL10 RPL22 RPL5 RPN1 RUNX1
More info about this panelTempus xO assay Panel
By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2
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 TUBGCP6 PXDN HCFC1 CNGB3 SBDS