Overview
Dent disease type 2 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.
Hypercalciuria
Always present (100%)HP:0002150
Low-molecular-weight proteinuria
Always present (100%)HP:0003126
Alanine aminotransferase increased
Frequent (30-79%)HP:0031964
Elevated circulating creatine phosphokinase
Frequent (30-79%)HP:0003236
Elevated serum aspartate aminotransferase
Frequent (30-79%)HP:0031956
Hypophosphataemia
Frequent (30-79%)HP:0002148
Increased lactate dehydrogenase level
Frequent (30-79%)HP:0025435
Increased levels of animo acids in urine
Frequent (30-79%)HP:0003355
Psychomotor retardation, mild
Frequent (30-79%)HP:0011342
Decreased body height
Occasional (5-29%)HP:0004322
Increased calcium level in kidney
Occasional (5-29%)HP:0000121
Umbilical hernia
Occasional (5-29%)HP:0001537
CKD
HP:0012622
Cognitive deficits
HP:0100543
Selective proximal tubular damage
HP:0000114
Related Conditions
Quick Facts
- SNOMED CT
- 717790004
- UMLS CUI
- C1845167
- Fully Specified Name
- Dent disease type 2 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 15
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.