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Living with Glaucoma type 1C

A condition that GARD doesn't have detailed information about yet.

Understanding Glaucoma type 1C

Glaucoma type 1C is a rare condition that GARD does not yet have detailed information about.

GARD does not currently have detailed information on this condition. Its Information Specialists are available to help people find information and resources, and to offer support on a diagnostic journey. GARD lists autosomal dominant inheritance.

Signs & symptoms

GARD doesn't list specific symptoms for this condition yet.

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Your doctor may refer you to a specialist who knows rare conditions.

  3. Ask which tests can help

    Your care team will decide which exams and tests can confirm the diagnosis.

Care & treatment

Care team
A doctor familiar with rare conditions, plus specialists as needed
Expert care
Ask about multidisciplinary care centers for rare conditions
Treatment
GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
Research
Clinical trials and observational studies may be options. See the research section below.

General information, not medical advice. Your care team makes the decisions.

Everyday life

Living with a rare condition is easier with support.

  • Connect with Prevent Blindness America
  • Keep notes on symptoms, changes and questions for appointments
  • Ask about patient registries that help research
  • Look into financial aid and travel resources for care visits
Bring these questions to your next doctor visit
How is this type of glaucoma different from other types?
How often should my eye pressure and vision be checked?
Should my family members have eye exams?

Quick facts

InheritanceAutosomal Dominant

GARD doesn't describe a cause for this condition yet. It lists autosomal dominant inheritance, which means one changed copy of a gene can be enough.

Also known as: glaucoma 1, primary open angle, c; glaucoma 1c, primary open angle

Patient organizations

Source: NIH GARD · Glaucoma type 1CGARD ID 2484 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with Glaucoma type 1C.

Explore the Glaucoma type 1C blog

Explore research for Glaucoma type 1C

Explore actively recruiting Glaucoma type 1C studies with HealthSpark.

HealthSpark

Find actively recruiting studies for Glaucoma type 1C with HealthSpark. Share your city to explore research near you.

  • Recruiting studies from ClinicalTrials.gov
  • Share your city to look for research near you
  • Eligibility is confirmed by the study team

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I can help you find recruiting Glaucoma type 1C studies. Enter a ZIP code, address or city below and I'll look within 50 miles.

Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.

Get Signals for Glaucoma type 1C

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HealthStoryfor Glaucoma type 1C

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