OrphanDrug
OrphanDrug
Pharma Knowledge Base

scalp–ear–nipple syndrome

MeSH: C536623ORPHA: 2036

Contents

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

Overview

human disease

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 scalp–ear–nipple syndrome, sourced from HPO and Orphanet clinical annotations.

Small earlobeAbnormality of the skinAbnormal scalp morphologyAplasia/Hypoplasia of the nipplesSparse hairMicrotiaAbnormal antihelix morphologyUnderdeveloped antitragusUnderdeveloped tragusBreast aplasiaRecurrent urinary tract infectionsAbnormality of the dentitionTelecanthusCataractDelayed eruption of teethHypertensionAbnormal fingernail morphologyPalpebral edemaType I diabetes mellitusUreteral duplicationAbnormality of the kidneyEyelid colobomaHypohidrosisDuplication of renal pelvisPyelonephritis

Classification & Codes

MeSH Code

C536623

Orphanet Code

ORPHA:2036
scalp–ear–nipple syndrome
MeSHC536623
OrphanetORPHA:2036
Treatments0 drug(s)
Symptoms on record25 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO