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.
Juvenile polyposis syndrome
Ehlers-Danlos syndrome, type 4
Very frequent (80-99%)
Romano-Ward syndrome
Very rare (1-4%)
Juvenile nephropathic cystinosis
Occasional (5-29%)
Poisoning by colchicine
Frequent (30-79%)
Congenital secretory diarrhea, chloride type
Always present (100%)
Proximal renal tubular acidosis
Frequent (30-79%)
Pineal hyperplasia AND diabetes mellitus syndrome
Occasional (5-29%)
Argininosuccinate lyase deficiency
Occasional (5-29%)
Nelson syndrome
Frequent (30-79%)
Glycogenosis with glucoaminophosphaturia
Frequent (30-79%)
Infantile nephropathic cystinosis
Very frequent (80-99%)
Cholera
Frequent (30-79%)
Cronkhite-Canada syndrome
Marburg virus disease
Occasional (5-29%)
Lowe syndrome
Frequent (30-79%)
Familial hypokalemic alkalosis, Gullner type
Leprechaunism syndrome
Occasional (5-29%)
Deficiency of steroid 11-beta-hydroxylase
Very frequent (80-99%)
Deficiency of steroid 17-alpha-hydroxylase
Frequent (30-79%)
Pituitary dependent hypercortisolism
Cystinosis
Very frequent (80-99%)
Type I renal tubular acidosis
Very frequent (80-99%)
De Toni-Fanconi syndrome
Frequent (30-79%)
Adult Fanconi syndrome
Excluded (<1%)
Quick Facts
- SNOMED CT
- 166690008
- UMLS CUI
- C0683388
- Fully Specified Name
- Serum potassium level below reference range (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.