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.
Cockayne syndrome
Occasional (5-29%)
Phytanic acid storage disease
Occasional (5-29%)
Familial dysautonomia
Megacalycosis
Frequent (30-79%)
Congenital microvillous atrophy
Frequent (30-79%)
Dalmatian hypouricaemia
Frequent (30-79%)
Upshaw-Schulman syndrome
Amyloid polyneuropathy type I
Frequent (30-79%)
Familial haemophagocytic lymphohistiocytosis
Frequent (30-79%)
Ring chromosome 13 syndrome
Occasional (5-29%)
Primary hyperoxaluria type 3
Very frequent (80-99%)
Acquired hemophagocytic lymphohistiocytosis associated with malignant disease
Very frequent (80-99%)
Congenital megacalycosis
Frequent (30-79%)
Well differentiated liposarcoma
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 39539005
- UMLS CUI
- C0151746
- Fully Specified Name
- Abnormal renal function (finding)
- Associated Conditions
- 14
- 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.