Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Nephrogenic diabetes insipidus
Always present (100%)HP:0009806
Hypernatremia
Very frequent (80-99%)HP:0003228
Hypernatremic dehydration
Very frequent (80-99%)HP:0004906
Hyposthenuria
Very frequent (80-99%)HP:0003158
Anorexia
Frequent (30-79%)HP:0002039
Constipation
Frequent (30-79%)HP:0002019
Extreme thirst
Frequent (30-79%)HP:0001959
Nausea and vomiting
Frequent (30-79%)HP:0002017
Poor weight gain
Frequent (30-79%)HP:0001508
Pyrexia
Frequent (30-79%)HP:0001945
Decreased body height
Occasional (5-29%)HP:0004322
Feeding difficulties
Occasional (5-29%)HP:0011968
Hypovolemia
Occasional (5-29%)HP:0011106
Poor bladder function
Occasional (5-29%)HP:0000009
Renal failure
Occasional (5-29%)HP:0000083
Retarded growth
Occasional (5-29%)HP:0001510
Seizures
Occasional (5-29%)HP:0001250
Uroureter
Occasional (5-29%)HP:0000072
Enuresis nocturna
Very rare (1-4%)HP:0010677
Hydramnios
Very rare (1-4%)HP:0001561
Mental and motor retardation
Very rare (1-4%)HP:0001263
Related Conditions
Acquired nephrogenic diabetes insipidus(child)
Partial nephrogenic diabetes insipidus(child)
Nephrogenic diabetes insipidus and intracranial calcification syndrome(child)
Hereditary vasopressin resistance(child)
Secondary arginine vasopressin resistance(child)
Vasopressin-related polyuria(parent)
Urinary system disease(parent)
Quick Facts
- SNOMED CT
- 111395007
- UMLS CUI
- C0162283
- Fully Specified Name
- Arginine vasopressin resistance (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 21
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.