MIR3681HG gene related symptoms and diseases
All the information presented here about the MIR3681HG gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to MIR3681HG gene
|Symptoms // Phenotype||% Cases|
|Respiratory distress||Very Common - Between 80% and 100% cases|
|Central apnea||Very Common - Between 80% and 100% cases|
|Abnormal respiratory system morphology||Very Common - Between 80% and 100% cases|
|Respiratory failure requiring assisted ventilation||Very Common - Between 80% and 100% cases|
|Pulmonary sequestration||Very Common - Between 80% and 100% cases|
Other less frequent symptoms and clinical featuresPatients with MIR3681HG gene alterations may also develop some of the following symptoms and phenotypes:
Commonly - More than 50% cases
- Functional respiratory abnormality
- Diaphragmatic paralysis
- Right ventricular failure
- Chronic lung disease
- Right ventricular hypertrophy
And 9 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to MIR3681HG gene
Here you will find a list of rare diseases related to the MIR3681HG. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
BRONCHOPULMONARY DYSPLASIA Is also known as bpd
Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome (see these terms) in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring.
Most common symptoms of BRONCHOPULMONARY DYSPLASIA
- Respiratory distress
- Small for gestational age
- Sleep disturbance
More info about BRONCHOPULMONARY DYSPLASIA