HAND2 gene related symptoms and diseases
All the information presented here about the HAND2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to HAND2 gene
Symptoms // Phenotype | % Cases |
---|---|
Growth delay | Very Common - Between 80% and 100% cases |
Double outlet right ventricle | Very Common - Between 80% and 100% cases |
Sinusitis | Very Common - Between 80% and 100% cases |
Increased body weight | Very Common - Between 80% and 100% cases |
Easy fatigability | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with HAND2 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Clubbing
- Heart murmur
- Preauricular pit
- Polycythemia
- Underdeveloped supraorbital ridges
- Poor appetite
- Hyperventilation
- Truncus arteriosus
And 39 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to HAND2 gene
Here you will find a list of rare diseases related to the HAND2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
TETRALOGY OF FALLOT
Description
Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.
Most common symptoms of TETRALOGY OF FALLOT
- Growth delay
- Muscle weakness
- Cryptorchidism
- Anemia
- Brachydactyly
More info about TETRALOGY OF FALLOT
Search interest in HAND2
Potential gene panels for HAND2 gene
Cardiovascular Diseases_General Panel Panel
By Health in Code Cardiovascular Diseases_General Panel that also includes the following genes: RIT1 MRPL3 RRAS RYR1 RYR2 SAR1B BLK SCN10A SCN1B SCN2B
More info about this panelCongenital heart diseases Panel Panel
By Health in Code Congenital heart diseases Panel that also includes the following genes: BRAF SOS1 TBX1 TBX20 TBX5 TFAP2B TNNI3 MED12 ZIC3 ACTA2
More info about this panelHAND2 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the HAND2 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 KCNV2 VAMP1 RPS6KA3 EFTUD2 RP9 LAS1L GNE