Overview
Prune belly syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Sluggish pupillary reaction
Always present (100%)HP:0030211
Xerostomia
Always present (100%)HP:0000217
Abnormality of the bladder
Very frequent (80-99%)HP:0000014
Abnormality of the ureter
Very frequent (80-99%)HP:0000069
Absent/small lungs
Very frequent (80-99%)HP:0006703
Aplasia of the abdominal wall musculature
Very frequent (80-99%)HP:0005199
Congenital obstructing posterior urethral membranes
Very frequent (80-99%)HP:0010957
Cryptorchidism
Very frequent (80-99%)HP:0000028
Decreased fertility
Very frequent (80-99%)HP:0000144
Ureteral dilatation
Very frequent (80-99%)HP:0000072
VUR
Very frequent (80-99%)HP:0000076
Decreased amniotic fluid index
Frequent (30-79%)HP:0001562
Decreased testicular size
Frequent (30-79%)HP:0008734
Dyschezia
Frequent (30-79%)HP:0002019
Multicystic kidney dysplasia
Frequent (30-79%)HP:0000003
Prune belly
Frequent (30-79%)HP:0004392
Renal failure
Frequent (30-79%)HP:0000083
Repeated bladder infections
Frequent (30-79%)HP:0000010
respiratory infections, recurrent
Frequent (30-79%)HP:0002205
Rib anomalies
Frequent (30-79%)HP:0000772
Abnormal spinal segmentation
Occasional (5-29%)HP:0003422
Abnormality of the uterus
Occasional (5-29%)HP:0000130
Absent anus
Occasional (5-29%)HP:0002023
Atria septal defect
Occasional (5-29%)HP:0001631
Cobb angle greater than ten degrees
Occasional (5-29%)HP:0002650
Congenital hip dislocations
Occasional (5-29%)HP:0001374
Fetal foot inversion
Occasional (5-29%)HP:0001762
Intellectual impairment
Occasional (5-29%)HP:0100543
Intestinal atresia
Occasional (5-29%)HP:0011100
Intestinal malrotation
Occasional (5-29%)HP:0002566
Related Conditions
Prune belly syndrome with pulmonic stenosis, mental retardation and deafness(child)
Hypogonadism with prune belly syndrome(child)
Hereditary disorder of musculoskeletal system(parent)
Genitourinary congenital anomalies(parent)
Congenital absence of abdominal muscle(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 5187006
- UMLS CUI
- C0033770
- Fully Specified Name
- Prune belly syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.