autosomal dominant hypohidrotic ectodermal dysplasia

ORPHA: 1810

Contents

1. Overview
2. Available Treatments
3. Clinical Presentation
4. Classification & Codes

Overview

Autosomal dominant form of hypohidrotic ectodermal dysplasia

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 autosomal dominant hypohidrotic ectodermal dysplasia, sourced from HPO and Orphanet clinical annotations.

Abnormality of the dentitionHypodontiaThin skinHypohidrosisSparse body hairPremature loss of primary teethAbnormal dental morphologySparse hairAbnormal fingernail morphologyDepressed nasal ridgeEczematoid dermatitisAbnormality of skin pigmentationMalignant hyperthermiaProminent foreheadThick vermilion border

Classification & Codes

Orphanet Code

ORPHA:1810

autosomal dominant hypohidrotic ectodermal dysplasia

Orphanet	`ORPHA:1810`
Treatments	0 drug(s)
Symptoms on record	15 signs
Status	published

Factual Authority

Last Updated3/20/2026

Clinical DataHPO · Orphanet

Drug DataFDA · EMA · CDSCO