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camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye

MeSH: C535876ORPHA: 1323

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 camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye, sourced from HPO and Orphanet clinical annotations.

Narrow mouthNarrow palateFacial asymmetryMicrognathiaHigh foreheadStrabismusPtosisProptosisJoint stiffnessLow posterior hairlineScoliosisAbnormal calvaria morphologyAbnormal hip bone morphologyHyperlordosisVertebral segmentation defectShort statureBiparietal narrowingSynostosis of carpal bonesFinger syndactylyCamptodactyly of fingerAsymmetric growthIntrauterine growth retardation

Classification & Codes

MeSH Code

C535876

Orphanet Code

ORPHA:1323
camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye
MeSHC535876
OrphanetORPHA:1323
Treatments0 drug(s)
Symptoms on record22 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO