Schöpf–Schulz–Passarge syndrome

ICD-10: Q82.8MeSH: C565607ORPHA: 221039

Contents

1. Overview
2. Available Treatments
3. Classification & Codes

Overview

SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

ICD-10 Code

Q82.8

MeSH Code

C565607

Orphanet Code

ORPHA:221039

Schöpf–Schulz–Passarge syndrome

ICD-10	`Q82.8`
MeSH	`C565607`
Orphanet	`ORPHA:221039`
Treatments	0 drug(s)
Status	published

Factual Authority

Last Updated3/20/2026

Clinical DataHPO · Orphanet

Drug DataFDA · EMA · CDSCO