hypotrichosis
MeSH: D007039ORPHA: 55654
Overview
hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has material basis in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hypotrichosis, sourced from HPO and Orphanet clinical annotations.
Sparse eyelashesAlopeciaSparse scalp hairSparse body hairSparse eyebrowSparse hair
Classification & Codes
MeSH Code
D007039Orphanet Code
ORPHA:55654hypotrichosis
| MeSH | D007039 |
| Orphanet | ORPHA:55654 |
| Treatments | 0 drug(s) |
| Symptoms on record | 6 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO