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.
Mirizzi's syndrome
Frequent (30-79%)
Hereditary coproporphyria
Frequent (30-79%)
Glycogen storage disease, type V
Frequent (30-79%)
Acute intermittent porphyria
Occasional (5-29%)
Delta-4-3-oxosteroid-5-beta-reductase deficiency
Frequent (30-79%)
Homogentisicaciduria
Frequent (30-79%)
Systemic lupus erythematosus of childhood
Occasional (5-29%)
Genetic recurrent myoglobinuria
Very frequent (80-99%)
Navajo neuropathy
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 39575007
- UMLS CUI
- C0426396
- Fully Specified Name
- Urine looks dark (finding)
- Associated Conditions
- 9
- 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.