alopecia, androgenetic, 1 (AGA1) - Symptoms, Causes & Research | Kisho | Kisho

alopecia, androgenetic, 1

Rare Disease

MONDO:0007184

Also known as:

AGA1alopecia, androgenetic, 1baldness, Male pattern

Genes

–

Clinical Trials

3 active

Newborn Screening

–

Patient Groups

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Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Last reviewed: Feb 2026

Evidence base: Early

Find Clinical TrialsTrials

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 6, 2026

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 6, 2026

Overview

Limited structured data is available for this condition. Information continues to be gathered as research progresses.(3 data sources · Data coverage: Limited)

Overview

Alopecia, androgenetic, 1 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

The condition is also known as AGA1 and is commonly referred to as male pattern baldness. There are currently no orphan drugs under investigation for this condition, and no information is available regarding inheritance patterns or associated symptoms.

Prognosis & Outlook

Patients and caregivers are encouraged to seek genetic counseling to understand potential hereditary aspects of the condition. Connecting with rare disease registries such as NORD or Orphanet may provide additional resources and support. Finding specialists experienced with alopecia or related conditions can also be beneficial.

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Clinical

Limited Clinical Data

Clinical profile data for this condition is not yet available. Phenotype information may still be loading below.

Treatment

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 6, 2026

Support

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:109200

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AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.

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alopecia, androgenetic, 1

Patient-Friendly Information

Clinical Trials

Clinical Trials

Overview

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Clinical

Limited Clinical Data

Treatment

Clinical Trials

Support

External Resources

OMIM

Related Diseases

Know a Patient Advocacy Group for this condition?

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