PAGOD syndrome
MeSH: C537018ORPHA: 991
Overview
PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital 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 PAGOD syndrome, sourced from HPO and Orphanet clinical annotations.
Abnormal morphology of female internal genitaliaPulmonary hypoplasiaAbnormality of the pulmonary arteryPulmonary artery hypoplasiaAbnormal cardiovascular system morphologyMulticystic kidney dysplasiaAbnormal testis morphologyAmbiguous genitaliaAbnormality of the uterusCongenital diaphragmatic herniaOmphaloceleHypoplastic left ventricleAgonadismRenal hypoplasia/aplasiaFemale pseudohermaphroditismMicrocephalyOptic atrophyAbnormal rib morphologyAbnormal clavicle morphologySudden cardiac deathAbnormal aortic morphologySitus inversus totalisAbnormality of the spleenEncephaloceleAbnormality of neuronal migrationSpina bifidaMeningoceleShort statureArrhythmiaAsymmetric growth
Classification & Codes
MeSH Code
C537018Orphanet Code
ORPHA:991PAGOD syndrome
| MeSH | C537018 |
| Orphanet | ORPHA:991 |
| Treatments | 0 drug(s) |
| Symptoms on record | 30 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO