Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Increased amniotic fluid index
Very frequent (80-99%)HP:0001561
Increased distance between eyes
Very frequent (80-99%)HP:0000316
Joint ligamentous laxity
Very frequent (80-99%)HP:0001382
Multiple kidney cysts
Very frequent (80-99%)HP:0005562
Poorly developed lungs
Very frequent (80-99%)HP:0002089
Premature birth
Very frequent (80-99%)HP:0001622
Renotubular dysgenesis
Very frequent (80-99%)HP:0008660
Selective proximal tubular damage
Very frequent (80-99%)HP:0000114
Bilateral single transverse palmar creases
Occasional (5-29%)HP:0007598
Decreased amniotic fluid index
Occasional (5-29%)HP:0001562
Decreased size of cranium
Occasional (5-29%)HP:0000252
Kidney damage
Occasional (5-29%)HP:0000112
Tetrology of fallot
Occasional (5-29%)HP:0001636
Abnormality of the urinary system
HP:0000079
Absent urine output
HP:0100519
Hypotension
HP:0002615
Potter facies
HP:0002009
Respiratory insufficiency
HP:0002093
Widely patent fontanelles and sutures
HP:0004492
Quick Facts
- SNOMED CT
- 702397002
- UMLS CUI
- C0266313
- Fully Specified Name
- Renal tubular dysgenesis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 19
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.