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 features

Patients with MIR3681HG gene alterations may also develop some of the following symptoms and phenotypes:

• Commonly - More than 50% cases

• Tracheobronchomalacia
• Functional respiratory abnormality
• Diaphragmatic paralysis
• Right ventricular failure
• Atelectasis
• Chronic lung disease
• Dyspnea
• 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.

Search interest in MIR3681HG

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