JSON

PAGOD syndrome

^ http://purl.obolibrary.org/obo/MONDO_0008741

PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies. [ Orphanet:991 ]

Term info

database cross reference
  • MESH:C537018 (MONDO:equivalentTo)
  • Orphanet:991 (OMIM:202660)
  • UMLS:C1859967 (OMIM:202660)
  • SCTID:722132007 (MONDO:equivalentTo)
  • OMIM:202660 (Orphanet:991/e)
  • GARD:0003086 (MONDO:equivalentTo)
Subsets

ordo_malformation_syndrome

definition

PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies.

exactMatch

http://identifiers.org/mesh/C537018, http://linkedlifedata.com/resource/umls/id/C1859967, http://purl.obolibrary.org/obo/Orphanet_991, http://identifiers.org/snomedct/722132007, https://omim.org/entry/202660

has exact synonym

PAGOD syndrome, pulmonary hypoplasia-agonadism-dextrocardia-diaphragmatic hernia syndrome

has related synonym

Kennerknecht sorgo Oberhoffer syndrome, agonadism with multiple internal malformations, pulmonary hypoplasia, hypoplasia of the pulmonary artery, agonadism, omphalocele-diaphragmatic defect, and dextrocardia

id

MONDO:0008741