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.
Table of contents:
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
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
Search interest in MMP19
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 United States.
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