PAGOD syndrome
MONDO:0008741Mondo
Findings
No curated finding names PAGOD syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies.
Definition from the Mondo Disease Ontology (MONDO:0008741), read 2026-09-29. CC BY 4.0.
- Onset and course
- Death in infancy
HPO, annotations 2026-09-02
Features
30 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal cardiovascular system morphologyHPOHP:0030680
- Very frequent (80% to 99% of cases)
- Abnormal morphology of female internal genitaliaHPOHP:0000008
- Very frequent (80% to 99% of cases)
- Abnormality of the pulmonary arteryHPOHP:0004414
- Very frequent (80% to 99% of cases)
- Pulmonary artery hypoplasiaHPOHP:0004971
- Very frequent (80% to 99% of cases)
- Pulmonary hypoplasiaHPOHP:0002089
- Very frequent (80% to 99% of cases)
- Abnormal testis morphologyHPOHP:0000035
- Frequent (30% to 79% of cases)
Show the remaining 18
- Multicystic kidney dysplasiaHPOHP:0000003
- Frequent (30% to 79% of cases)
- OmphaloceleHPOHP:0001539
- Frequent (30% to 79% of cases)
- Renal hypoplasia/aplasiaHPOHP:0008678
- Frequent (30% to 79% of cases)
- Abnormal aortic morphologyHPOHP:0001679
- Occasional (5% to 29% of cases)
- Abnormal clavicle morphologyHPOHP:0000889
- Occasional (5% to 29% of cases)
- Abnormal rib morphologyHPOHP:0000772
- Occasional (5% to 29% of cases)
Where it sits
Other names
1 name
Resolves to: PAGOD syndrome
- Also called
- pulmonary hypoplasia-agonadism-dextrocardia-diaphragmatic hernia syndrome