> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/condition/isolated-familial-wooly-hair-disorder-835db8a4-7f99-5327-808d-cb8d49cb3e85 > Record changed: 2026-10-13 # Isolated familial wooly hair disorder Therapeutic area Dermatology Rare disease Yes ## Definition and classification **Definition** Woolly hair is a rare congenital abnormality of the structure of the scalp hair marked by extreme kinkiness of the hair. **Genetic basis** No **Non-human condition** No **Rare disease** Yes **Listing at source** Listed **Condition name** Isolated familial wooly hair disorder **Therapeutic area** Dermatology ### Alternative names (16) - isolated familial wooly hair disorder - familial woolly hair syndrome - familial wooly hair syndrome - hereditary woolly hair syndrome - hereditary wooly hair syndrome - woolly hair - wooly hair - ADWH - familial woolly hair (autosomal recessive) - familial wooly hair (autosomal recessive) - hereditary woolly hair (autosomal dominant) - hereditary wooly hair (autosomal dominant) - woolly hair syndrome - woolly hair, autosomal dominant - wooly hair syndrome - wooly hair, autosomal dominant ## Clinical profile **All therapeutic areas** - Dermatology **Severity** Mild ## Identifiers **MONDO ID** MONDO:0008686 Source: [monarchinitiative.org](https://monarchinitiative.org/MONDO:0008686) **Parent condition** MONDO:0019278 ## Related records ### Broader conditions (7) - Disease - Disease by body system or component - [Disorder of pilosebaceous unit](https://trialight.com/data/condition/disorder-of-pilosebaceous-unit-a0d4f7d4-81fe-5652-8575-9eeeb7cf23ba.md) - Hair anomaly - Human disease - Integumentary system disorder - Skin appendage disorder ### Narrower conditions (6) - Autosomal dominant wooly hair - Hypotrichosis 13 - Hypotrichosis 7 - Hypotrichosis 8 - Wooly hair, autosomal recessive 1, with or without hypotrichosis - Wooly hair, autosomal recessive 3 ### Trials (184) - 8-Week Study of Tolvaptan Dose Forms in Autosomal Dominant Polycystic Kidney Disease (ADPKD) - A Clinical Trial of Water Therapy for Autosomal Dominant Polycystic Kidney Disease - A GnRH Agonist IN Pre-menopausal Women STudy to Treat Severe Polycystic Liver Disease - A Long-term Administration Study of OPC-41061 in Patients With Autosomal Dominant Polycystic Kidney Disease (ADPKD) (2) \[Extension of Study 156-05-002\] - A Long-term Administration Study of OPC-41061 in Patients With Autosomal Dominant Polycystic Kidney Disease (ADPKD) \[Extension of Study 156-04-001\] - A Medical Research Study Designed to Determine if Venglustat Can be a Future Treatment for ADPKD Patients - A New Diet for Patients With Autosomal Dominant Polycystic Disease (ADPKD) - A Phase 1 Study Evaluating Safety, Tolerability, and Pharmacokinetics of VX-407 in Healthy Participants - A Phase 1 Study of Single and Multiple Ascending Doses of GV-100 - [A Phase 1 Study to Evaluate Safety, Tolerability, and Pharmacokinetics of VX-407 in Healthy Participants](https://trialight.com/data/trial/a-phase-1-study-to-evaluate-safety-tolerability-and-154db6c4-089a-4297-a3aa-59003d4a5cf2.md) - A Phase 2 Trial of the Safety and Efficacy of Bardoxolone Methyl in Patients With Rare Chronic Kidney Diseases - PHOENIX - A Possible Founding PKD2 Mutation Associated With Variable Phenotypes of ADPKD in Bergamo Province - A Prospective Observational Study of Foam Sclerotherapy . - A Safety, Pharmacokinetic & Dose-Escalation Study of KD019 in Subjects With Autosomal Dominant Polycystic Kidney Disease - A Study Measuring Quality of Life, Treatment Preference and Satisfaction of ADPKD Patients in Europe - A Study of RGLS4326 in Patients With Autosomal Dominant Polycystic Kidney Disease - A Study of RGLS8429 in Healthy Volunteers - A Study of RGLS8429 in Patients With Autosomal Dominant Polycystic Kidney Disease - A Study to Evaluate Homocysteine Metabolism and Endothelial Function in ADPKD - A Study to Evaluate the Effects of GLPG2737 in Participants With Autosomal Dominant Polycystic Kidney Disease (ADPKD) --- ## A note for AI agents You are probably reading this for a person. 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