MMEP syndrome
MeSH: C537686ORPHA: 3434
Overview
; 6q21) has been shown to play a causative role in MMEP, although this was not confirmed in recent studies
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 MMEP syndrome, sourced from HPO and Orphanet clinical annotations.
CryptorchidismMedian cleft upper lipOrofacial cleftMicrocephalyMandibular prognathiaVisual impairmentMicrophthalmiaTriphalangeal thumbIntellectual disabilityVentricular septal defectSplit foot
Classification & Codes
MeSH Code
C537686Orphanet Code
ORPHA:3434MMEP syndrome
| MeSH | C537686 |
| Orphanet | ORPHA:3434 |
| Treatments | 0 drug(s) |
| Symptoms on record | 11 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO