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PAGOD syndrome

Disease Summary
Associated Targets (0)

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Mondo Description PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies.
Mondo Term and Equivalent IDs
MONDO:0008741:  PAGOD syndrome
GARD:0003086: 
MESH:C537018: 
Orphanet:991: 
SCTID:722132007: 
UMLS:C1859967: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found