Glaucoma, Normal Tension, Susceptibility To
Genes related to Glaucoma, Normal Tension, Susceptibility To
- OPTN
 - OPA1
 
Clinical Features
Phenotypes and symptoms related to Glaucoma, Normal Tension, Susceptibility To
- Blindness
 - Glaucoma
 - Increased intraocular pressure
 - 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.
Alternative names
Glaucoma, Normal Tension, Susceptibility To Is also known as npg, ntg, glaucoma, normal pressure, susceptibility to.
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, Normal Tension, Susceptibility To Recommended genes panels
| Panel Name, Specifity and genes Tested/covered | 
|---|
 	MitoMet®Plus aCGH Analysis.
By Baylor Miraca Genetics Laboratories (United States). 
RGS9, RHO, GRK1, RLBP1, RNASEL, BCS1L, RP1, RP2, RP9, RPE65, RPGR, RPL35A, MRPL3, RPS14, RS1, SAG, SARDH, SCO2, SCP2, SDHB	, (...)
 
View the complete list with 612 more genes 
Specificity
 
1 % 
Genes
 
100 %  | 
 	Amyotrophic Lateral Sclerosis Advanced Evaluation.
By Athena Diagnostics Inc (United States). 
SOD1, SQSTM1, TARDBP, UBQLN2, VAPB, VCP, FIG4, OPTN, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, ANG, SIGMAR1, PFN1
 
Specificity
 
6 % 
Genes
 
50 %  | 
 	Nonprevalent Amyotrophic Lateral Sclerosis Advanced Sequencing Evaluation.
By Athena Diagnostics Inc (United States). 
SQSTM1, TARDBP, UBQLN2, VAPB, VCP, FIG4, OPTN, CHMP2B, DCTN1, FUS, ALS2, SETX, ANG, SIGMAR1, PFN1
 
Specificity
 
7 % 
Genes
 
50 %  | 
 	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
 
6 % 
Genes
 
100 %  | 
 	Amyotrophic Lateral Sclerosis.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). 
ATXN2, SOD1, TARDBP, UBQLN2, VAPB, VCP, VEGFA, FIG4, OPTN, SPART, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, ANG, NEFH, SIGMAR1, PFN1	, (...)
 
View the complete list with 1 more genes 
Specificity
 
5 % 
Genes
 
50 %  | 
 	Dementia.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). 
SORL1, TARDBP, VCP, FIG4, OPTN, TREM2, CSF1R, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, GRN, ANG, APOE, APP, MAPT, PRNP, PSEN1	, (...)
 
View the complete list with 1 more genes 
Specificity
 
5 % 
Genes
 
50 %  | 
 	Primary Open Angle Glaucoma (Adult onset).
By Medical Genetics Laboratory, Kennedy Center Juliane Marie Center, Rigshospitalet (Denmark). 
OPTN, WDR36, MYOC
 
Specificity
 
34 % 
Genes
 
50 %  | 
 	OPTN Gene Sequencing.
By GeneDx (United States). 
OPTN
 
Specificity
 
100 % 
Genes
 
50 %  | 
You can get up to 148 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS; RAMSVPS BARDET-BIEDL SYNDROME 13; BBS13 APERT SYNDROME LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9 MUCOPOLYSACCHARIDOSIS, TYPE IIIB; MPS3B BRANCHIOOTORENAL SYNDROME 2; BOR2 AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18
	MitoMet®Plus aCGH Analysis.
	Primary Open Angle Glaucoma (Adult onset).