SSUH2 gene related symptoms and diseases

All the information presented here about the SSUH2 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 SSUH2 gene

Symptoms // Phenotype	% Cases
Carious teeth	Very Common - Between 80% and 100% cases
Delayed eruption of teeth	Very Common - Between 80% and 100% cases
Microdontia	Very Common - Between 80% and 100% cases
Increased bone mineral density	Very Common - Between 80% and 100% cases
Oligodontia	Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with SSUH2 gene alterations may also develop some of the following symptoms and phenotypes:

• Commonly - More than 50% cases

• Open bite
• Taurodontia
• Generalized osteosclerosis
• Anterior open bite
• Pulp stones
• Dentinogenesis imperfecta limited to primary teeth
• No permanent dentition
• Periapical bone loss

And 3 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to SSUH2 gene

Here you will find a list of rare diseases related to the SSUH2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.

Search interest in SSUH2

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like BCL3 NR1I2 TONSL NNT JAK2 SUGCT TRAPPC9