Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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ORPHA:90794OMIM:201910E25.0
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8Treatment centers

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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:

Increased circulating androgen concentrationHP:0030348Abnormal response to ACTH stimulation testHP:0031074Elevated circulating 17-hydroxyprogesterone concentrationHP:0031213Increased circulating progesteroneHP:0031216Renal salt wastingHP:0000127Abnormality of the menstrual cycleHP:0000140Abnormal external genitalia morphologyHP:0000811Hyperactive renin-angiotensin systemHP:0000841Growth abnormalityHP:0001507Neonatal hypoglycemiaHP:0001998
Orphanet ↗OMIM ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

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No actively recruiting trials found for Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency at this time.

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No specialists are currently listed for Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

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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 Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

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Community

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