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Campomelia, Cumming type

MeSH: C537966ORPHA: 1318

Contents

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

Overview

Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies

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 Campomelia, Cumming type, sourced from HPO and Orphanet clinical annotations.

Multicystic kidney dysplasiaCleft palateDolichocephalyCystic hygromaAbnormal rib morphologyBrachydactylyOligohydramniosAbnormality of the pancreasPancreatic cystsSkeletal dysplasiaMicromeliaMultiple renal cystsBowing of the long bonesPrematurely aged appearanceClubbing of toesAbnormal thorax morphologyHydrops fetalisHepatomegalyMyelodysplasiaSkin dimpleAbnormally ossified vertebraeCoarse facial featuresLymphedemaAbnormal intestine morphologyAplasia/Hypoplasia affecting the eyeAbnormal cardiovascular system morphology

Classification & Codes

MeSH Code

C537966

Orphanet Code

ORPHA:1318
Campomelia, Cumming type
MeSHC537966
OrphanetORPHA:1318
Treatments0 drug(s)
Symptoms on record26 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO