DLX4 gene related symptoms and diseases

All the information presented here about the DLX4 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,ORPHANET,OMIM,HGNC, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to DLX4 gene

Symptoms // Phenotype	% Cases
Hypertelorism	Uncommon - Between 30% and 50% cases
Sparse eyebrow	Uncommon - Between 30% and 50% cases
Palate fistula	Uncommon - Between 30% and 50% cases
Agenesis of lateral incisor	Uncommon - Between 30% and 50% cases
Bilateral cleft palate	Uncommon - Between 30% and 50% cases

Other less frequent symptoms and clinical features

Patients with DLX4 gene alterations may also develop some of the following symptoms and phenotypes:

• Not very common - Between 30% and 50% cases

• Euryblepharon
• Ectropion of lower eyelids
• High anterior hairline
• Bilateral cleft lip and palate
• Bilateral cleft lip
• Ectropion
• Sparse eyelashes
• Abnormal facial shape

And 11 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to DLX4 gene

Here you will find a list of rare diseases related to the DLX4. You can also use our tool to get a more accurate diagnosis based on your current symptoms.

Search interest in DLX4

Potential gene panels for DLX4 gene

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