OrphanDrug
OrphanDrug
Pharma Knowledge Base

congenital rubella syndrome

ICD-10: P35.0MeSH: D012410ORPHA: 290

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 congenital rubella syndrome, sourced from HPO and Orphanet clinical annotations.

Abnormal cranial suture/fontanelle morphologyMicrocephalySensorineural hearing impairmentStrabismusGlaucomaVisual impairmentCataractMicrophthalmiaNystagmusAbnormal metaphysis morphologyJaundiceSkin rashIntellectual disabilitySeizureHypotoniaSpastic diplegiaIntrauterine growth retardationVentricular septal defectAtrial septal defectPatent ductus arteriosusSplenomegalyThrombocytopeniaAnemiaAbnormal speech patternHepatomegalyShort statureAbnormality of the pulmonary arteryAbnormal retinal pigmentationCorneal opacityAplasia/Hypoplasia of the irisType I diabetes mellitus

Classification & Codes

ICD-10 Code

P35.0

MeSH Code

D012410

Orphanet Code

ORPHA:290
congenital rubella syndrome
ICD-10P35.0
MeSHD012410
OrphanetORPHA:290
Treatments0 drug(s)
Symptoms on record31 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO