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Personal Solutions
Eye Disorder Panel
Eye disorder genetic testing involves examining an individual's genetic makeup to identify specific genetic variations linked to various eye conditions. It aims to uncover inherited markers that could increase the risk of developing eye disorders. This test provides insights into genetic predispositions, aiding in early detection, personalized risk assessment, and tailored preventive measures.
Genes and Eye Conditions
Outlining key gene mutations associated with various eye disorder conditions. Understanding the genetic basis of these disorders is crucial for early diagnosis, personalized treatment strategies, and advancing our knowledge of ocular genetics.
Conditions | Genes |
|---|---|
Retinitis Pigmentosa | BEST1, NR2E3, NRL, RHO, RP1, RPE65 |
Cataracts | ALDH7A1, BFSP1, BFSP2, CAV1, CRYAA, CRYAB, CRYGC, CTSD, CYP1B1, FTL, GALK1, HSF4, SLC2A1, TGFBI |
Glaucoma | CAV1, CAV2, CDKN2B-AS, FOXC1, FOXE3, PAX6, PITX2, SIX1, SIX6, TMCO1 |
Colorblindness | OPN1LW, OPN1MW |
Personal Solutions
LIFESTYLE GENETICS PANEL
PHARMACOGENOMICS PANEL
CANCER RISK PANEL
CARDIAC RISK PANEL
DIABETES RISK PANEL
NEUROLOGY RISK PANEL
IMMUNODEFICIENCY PANEL
EYE DISORDER PANEL
ANEMIA PANEL
ANNUAL CHECK-UP PANEL
ARTHRITIS SCREENING PANEL
BASIC NUTRITIONAL PANEL
BASIC STD PANEL
CHOLESTEROL (LIPID) PANEL
CHOLESTEROL MEDICATION MAINTENANCE PANEL
COMPREHENSIVE METABOLIC PANEL
DIABETES MAINTENANCE PANEL
ELECTROLYTE PANEL
HEART HEALTH PANEL
OSTEOPOROSIS RISK PANEL
PRENATAL OB PANEL
RENAL FUNCTION PANEL
SEMAGLUTIDE MONITORING PANEL
STD PANEL, COMPREHENSIVE
TESTOSTERONE PANEL (CONTINUED-THERAPY)
THYROID PANEL
ALLERGY PANEL
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