OGT gene related symptoms and diseases

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

Top 5 symptoms and clinical features associated to OGT gene

Symptoms // Phenotype	% Cases
Intellectual disability	Very Common - Between 80% and 100% cases
Wide nose	Very Common - Between 80% and 100% cases
Slender finger	Very Common - Between 80% and 100% cases
High hypermetropia	Very Common - Between 80% and 100% cases
Supernumerary nipple	Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

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

• Commonly - More than 50% cases

• Spastic diplegia
• Drooling
• Bicuspid aortic valve
• Finger clinodactyly
• Amblyopia
• Open mouth
• Narrow forehead
• Decreased testicular size

And 16 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to OGT gene

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

Search interest in OGT

Potential gene panels for OGT gene

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