MCM5 gene related symptoms and diseases

All the information presented here about the MCM5 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to MCM5 gene

Symptoms // Phenotype	% Cases
Micrognathia	Very Common - Between 80% and 100% cases
Cryptorchidism	Very Common - Between 80% and 100% cases
Ptosis	Very Common - Between 80% and 100% cases
Low-set ears	Very Common - Between 80% and 100% cases
Narrow mouth	Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with MCM5 gene alterations may also develop some of the following symptoms and phenotypes:

• Commonly - More than 50% cases

• Microtia
• Thick vermilion border
• Renal hypoplasia
• Bilateral cryptorchidism

Rare diseases associated to MCM5 gene

Here you will find a list of rare diseases related to the MCM5. You can also use our tool to get a more accurate diagnosis based on your current symptoms.

Search interest in MCM5

Potential gene panels for MCM5 gene

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