MMP19 gene related symptoms and diseases

All the information presented here about the MMP19 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE,OMIM,ORPHANET, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to MMP19 gene

Symptoms // Phenotype % Cases
Glaucoma Very Common - Between 80% and 100% cases
Reduced visual acuity Very Common - Between 80% and 100% cases
Coloboma Very Common - Between 80% and 100% cases
Nyctalopia Very Common - Between 80% and 100% cases
Visual field defect Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with MMP19 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Increased intraocular pressure
  • Morning glory anomaly
  • Peripapillary atrophy
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Rare diseases associated to MMP19 gene

Here you will find a list of rare diseases related to the MMP19. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


FAMILIAL CAVITARY OPTIC DISC ANOMALY


Alternate names

FAMILIAL CAVITARY OPTIC DISC ANOMALY Is also known as familial coda

Most common symptoms of FAMILIAL CAVITARY OPTIC DISC ANOMALY

  • Glaucoma
  • Reduced visual acuity
  • Coloboma
  • Nyctalopia
  • Visual field defect


More info about FAMILIAL CAVITARY OPTIC DISC ANOMALY

SOURCES: MESH OMIM ORPHANET


Potential gene panels for MMP19 gene

MMP19 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the MMP19 gene.

More info about this panel


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