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.
Ulcerative cystitis
Very frequent (80-99%)
Microcephaly, normal intelligence and immunodeficiency
Frequent (30-79%)
Fragile X associated tremor ataxia syndrome
Frequent (30-79%)
Autosomal recessive limb girdle muscular dystrophy type 2B
Very rare (1-4%)
Autosomal recessive facio-digito-genital syndrome
Occasional (5-29%)
Primary hyperoxaluria type 3
Very frequent (80-99%)
Autosomal recessive spastic paraplegia type 35
Occasional (5-29%)
Cataracts, motor neuropathy, short stature, skeletal anomalies syndrome
Occasional (5-29%)
Autosomal recessive spastic paraplegia type 9B
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 300471006
- UMLS CUI
- C0042023
- Fully Specified Name
- Finding of frequency of urination (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.