Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Paroxysmal nocturnal hemoglobinuria
Very rare (1-4%)
Hereditary fructosuria
Juvenile nephropathic cystinosis
Frequent (30-79%)
Glutaric aciduria, type 2
Proximal renal tubular acidosis
Occasional (5-29%)
Glycogenosis with glucoaminophosphaturia
Frequent (30-79%)
Infantile nephropathic cystinosis
Very frequent (80-99%)
Cytochrome-c oxidase deficiency
Wilson's disease
Myasthenia gravis
Occasional (5-29%)
Cystinosis
Frequent (30-79%)
Glucose-galactose malabsorption
Westphal-Strumpell syndrome
Familial renal glucosuria
Always present (100%)
De Toni-Fanconi syndrome
Very frequent (80-99%)
Adult Fanconi syndrome
Always present (100%)
Insulin resistance - type B
Frequent (30-79%)
Pearson's syndrome
Occasional (5-29%)
Familial hypoplastic, glomerulocystic kidney
Frequent (30-79%)
Bilateral renal hypoplasia
Occasional (5-29%)
Dent disease
Very frequent (80-99%)
Maturity-onset diabetes of the young
Frequent (30-79%)
Permanent diabetes mellitus of infancy
Very frequent (80-99%)
Maturity-onset diabetes of the young, type 5
Frequent (30-79%)
Atypical Werner syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 45154002
- UMLS CUI
- C0017979
- Fully Specified Name
- Glycosuria (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.