Hereditary angioedema type 1

Last reviewed

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ORPHA:100050OMIM:106100D84.1
Who is this for?
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18Specialists8Treatment centers

Where are you in your journey?

UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
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Overview

Also known as:

Clinical phenotype terms— hover any for plain English:

Intestinal edemaHP:0005225Edema of the dorsum of handsHP:0007514Dermatographic urticariaHP:0011971Laryngeal edemaHP:0012027Abnormal respiratory system morphologyHP:0012252Limbal edemaHP:0025349Tongue edemaHP:0040315Abnormality of salivationHP:0100755Abnormal uvula morphologyHP:0000172
Orphanet ↗OMIM ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Hereditary angioedema type 1.

View clinical trials →

No actively recruiting trials found for Hereditary angioedema type 1 at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Hereditary angioedema type 1 community →

Specialists

18 foundView all specialists →
MM
Marcus Maurer, MD
PUEBLO, CO
Specialist
PI on 5 active trials
GD
Global Clinical Program Director
Specialist
PI on 5 active trials
NB
Nora Contreras Bravo
Specialist
1 Hereditary angioedema type 1 publication
LC
Lilian Andrea Casas-Vargas
Specialist
1 Hereditary angioedema type 1 publication
LH
Laura Huilaja
Specialist
1 Hereditary angioedema type 1 publication
JA
Juan Sebastian Arias-Flórez
Specialist
1 Hereditary angioedema type 1 publication
SR
Sandra Ximena Ramirez
Specialist
1 Hereditary angioedema type 1 publication
VC
Valeria Correa-Martinez
Specialist
1 Hereditary angioedema type 1 publication
WU
William Usaquén-Martínez
Specialist
1 Hereditary angioedema type 1 publication
CO
Carlos Eduardo Olmos Olmos
COVINA, CA
Specialist
1 Hereditary angioedema type 1 publication
HP
Hilary Longhurst, MBBS, PhD
Specialist
PI on 1 active trial
YS
Yasmín Sanchez-Gomez
Specialist
1 Hereditary angioedema type 1 publication
LC
Lina Castro-Castillo
Specialist
1 Hereditary angioedema type 1 publication
IT
Iiro Toppila
Specialist
1 Hereditary angioedema type 1 publication
VV
Ville Vihervaara
Specialist
1 Hereditary angioedema type 1 publication
BB
Bibiana Bayona-Gomez
Specialist
1 Hereditary angioedema type 1 publication
ML
Mariann Lassenius
Specialist
1 Hereditary angioedema type 1 publication
AS
Andreas Sandberg
Specialist
1 Hereditary angioedema type 1 publication

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Hereditary angioedema type 1.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Hereditary angioedema type 1

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Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Common questions about Hereditary angioedema type 1

Which specialists treat Hereditary angioedema type 1?

18 specialists and care centers treating Hereditary angioedema type 1 are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.