Glaucoma 1, Open Angle, F; Glc1f

Clinical Features

Phenotypes and symptoms related to Glaucoma 1, Open Angle, F; Glc1f

  • Glaucoma
  • Visual field defect
  • Increased intraocular pressure
  • Open angle glaucoma
  • Glaucomatous visual field defect
  • Increased cup-to-disc ratio

Incidence and onset information

Not enough data available about incidence and published cases.
No data available about the known clinical features onset.

Alternative names

Glaucoma 1, Open Angle, F; Glc1f Is also known as glaucoma, primary open angle, adult-onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.


Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Glaucoma 1, Open Angle, F; Glc1f Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Optic Atrophy and Early Glaucoma Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

SLC4A4, SPG7, TBK1, ACO2, BEST1, WFS1, ACVR1, OPTN, ASB10, MFRP, CANT1, SBF2, COL4A1, CISD2, TMEM126A, MTPAP, CYP1B1, C12orf65, SH3PXD2B, FOXC1 , (...)

View the complete list with 14 more genes
Specificity
3 %
Genes
100 %
Glaucoma, open angle type 1F.

By Centogene AG - the Rare Disease Company (Germany).

ASB10
Specificity
100 %
Genes
100 %
Glaucoma.

By Asper Biogene Asper Biogene LLC (Estonia).

SLC4A4, BEST1, ACVR1, OPTN, ASB10, CANT1, SBF2, COL18A1, CYP1B1, WDR36, FOXC1, LMX1B, LOXL1, LTBP2, LTBP3, MYOC, NTF4, PAX6, PITX2, PITX3
Specificity
5 %
Genes
100 %
Glaucoma.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases (Spain).

RPGRIP1, OPTN, ASB10, OLFM2, MFRP, VSX2, COL8A2, CYP1B1, SH3PXD2B, WDR36, FOXC1, PRSS56, LOXL1, LTBP2, MYOC, NTF4, OPA1, OPTC, PAX6
Specificity
6 %
Genes
100 %
Glaucoma (Advance).

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases (Spain).

RPS19, SLC4A4, TTR, BEST1, RPGRIP1, CA4, ACVR1, OPTN, ASB10, OLFM2, RRM2B, MFRP, CANT1, VSX2, SBF2, COL18A1, COL8A2, CYP1B1, SH3PXD2B, WDR36 , (...)

View the complete list with 14 more genes
Specificity
3 %
Genes
100 %
ASB10.

By Fulgent Genetics Fulgent Genetics (United States).

ASB10
Specificity
100 %
Genes
100 %
GLAUCOMA, OPEN ANGLE.

By Laboratorio de Genetica Clinica SL (Spain).

OPTN, ASB10, WDR36, MYOC, NTF4
Specificity
20 %
Genes
100 %
GLAUCOMA NGS ÀNEL.

By Laboratorio de Genetica Clinica SL (Spain).

SLC4A4, TEK, BEST1, ACVR1, OPTN, ASB10, MFRP, CANT1, SBF2, COL18A1, COL4A1, COL8A2, CYP1B1, SH3PXD2B, WDR36, FOXC1, LMX1B, LOXL1, LTBP2, MYOC , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
100 %

We have 1 more panels available in our App

Get the app

Sources and references

You can check the following sources for additional information.

MESH OMIM Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE; MCPH5 MUIR-TORRE SYNDROME; MRTES PIERSON SYNDROME SPINOCEREBELLAR ATAXIA 34; SCA34 RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K WILSON DISEASE

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more