oculogastrointestinal muscular dystrophy
MeSH: C536350ORPHA: 1876
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 oculogastrointestinal muscular dystrophy, sourced from HPO and Orphanet clinical annotations.
Abnormal mitral valve morphologyMalabsorptionGastroparesisMyopathySkeletal muscle atrophyAbdominal distentionCachexiaIntestinal pseudo-obstructionAbnormality of the gastrointestinal tractPtosisExternal ophthalmoplegiaAbnormal gastric mucosa morphologySpontaneous esophageal perforation
Classification & Codes
MeSH Code
C536350Orphanet Code
ORPHA:1876oculogastrointestinal muscular dystrophy
| MeSH | C536350 |
| Orphanet | ORPHA:1876 |
| Treatments | 0 drug(s) |
| Symptoms on record | 13 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO