Glaucoma 1, Open Angle, G; Glc1g

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Glaucoma 1, Open Angle, G; Glc1g

WDR36

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Glaucoma 1, Open Angle, G; Glc1g

Open angle glaucoma

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features 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.

Glaucoma 1, Open Angle, G; Glc1g Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Primary Open Angle Glaucoma (Adult onset). By Medical Genetics Laboratory, Kennedy Center Juliane Marie Center, Rigshospitalet (Denmark). OPTN, WDR36, MYOC Specificity 34 % Genes 100 %
WDR36. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). WDR36 Specificity 100 % Genes 100 %
Glaucoma, open angle type 1G (sequence analysis of WDR36 gene). By CGC Genetics (Portugal). WDR36 Specificity 100 % Genes 100 %
Glaucoma Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SLC4A4, ATOH7, OPTN, MFRP, COL4A1, COL8A1, COL8A2, CYP1B1, SH3PXD2B, WDR36, FOXC1, LMX1B, LTBP2, MYOC, OPTC, PAX6, PITX2 Specificity 6 % Genes 100 %
Glaucoma, open angle type 1G. By Centogene AG - the Rare Disease Company (Germany). WDR36 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 Panel complete gene list RPS19, SLC4A4, TTR, BEST1, RPGRIP1, CA4, ACVR1, OPTN, ASB10, OLFM2, RRM2B, MFRP, CANT1, VSX2, SBF2, COL18A1, COL8A2, CYP1B1, SH3PXD2B, WDR36, ISPD, FOXC1, PRSS56, LMX1B, LOXL1, LTBP2, MTHFR, MYOC, NTF4, OPA1, OPTC, PAX6, PITX3, POMT1 Specificity 3 % Genes 100 %

You can get up to 8 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

MESH OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SEGMENTAL OUTGROWTH-LIPOMATOSIS-ARTERIOVENOUS MALFORMATION-EPIDERMAL NEVUS SYNDROME RETICULAR DYSGENESIS OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII; HMN8 AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3 SENGERS SYNDROME GAPO SYNDROME