Rapp-Hodgkin syndrome
MeSH: C535289ORPHA: 3022
Overview
autosomal dominant disease characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth and sweat glands and anhidrotic ectodermal dysplasia with cleft lip/palate
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C535289Orphanet Code
ORPHA:3022Rapp-Hodgkin syndrome
| MeSH | C535289 |
| Orphanet | ORPHA:3022 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO