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

D007039

Orphanet Code

ORPHA:55654
hypotrichosis
MeSHD007039
OrphanetORPHA:55654
Treatments0 drug(s)
Symptoms on record6 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO