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.
Pigmentary pallidal degeneration
Neuroleptic malignant syndrome
Occasional (5-29%)
Cockayne syndrome
Occasional (5-29%)
Sandhoff disease
Metachromatic leukodystrophy, adult type
Occasional (5-29%)
African trypanosomiasis
Occasional (5-29%)
Orthostatic hypotension
Arachnoid cyst
Occasional (5-29%)
Metachromatic leukodystrophy, congenital type
Frequent (30-79%)
Metachromatic leukodystrophy, juvenile type
Frequent (30-79%)
Acute transverse myelitis
Occasional (5-29%)
Metachromatic leukodystrophy, late infantile type
Frequent (30-79%)
Childhood absence epilepsy
Very rare (1-4%)
Alstrom syndrome
Occasional (5-29%)
Adrenoleukodystrophy
Occasional (5-29%)
Deficiency of cerebroside-sulfatase
Spina bifida
Sphingolipid activator protein 1 deficiency
Double urethra
Occasional (5-29%)
Childhood disintegrative disorder
Frequent (30-79%)
Gamma-glutamyl transpeptidase deficiency
Always present (100%)
Trypanosomiasis
Occasional (5-29%)
Bradbury-Eggleston syndrome
Chester-type porphyria
Hereditary sensory and autonomic neuropathy, type V
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 165232002
- UMLS CUI
- C0042024
- Fully Specified Name
- Urinary incontinence (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.