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.
Childhood type dermatomyositis
Occasional (5-29%)
Uhl's disease
Occasional (5-29%)
Typhoid fever
Frequent (30-79%)
Distichiasis-lymphedema syndrome
Occasional (5-29%)
Periodic disease
Occasional (5-29%)
Neuroleptic malignant syndrome
Occasional (5-29%)
Fabry's disease
Occasional (5-29%)
Glutaric aciduria, type 2
Very rare (1-4%)
AL amyloidosis
Occasional (5-29%)
Lyme disease
Occasional (5-29%)
Poisoning by colchicine
Frequent (30-79%)
Phytanic acid storage disease
Kearns-Sayre syndrome
Homozygous beta thalassemia
Very rare (1-4%)
African trypanosomiasis
Very rare (1-4%)
Schwartz-Jampel syndrome
Occasional (5-29%)
Ventricular septal defect
Occasional (5-29%)
Ehlers-Danlos syndrome, type 3
Frequent (30-79%)
Holoprosencephaly sequence
Occasional (5-29%)
Ectodermal dysplasia-ocular malformation syndrome
Occasional (5-29%)
Polymyositis
Occasional (5-29%)
Sarcoidosis
Occasional (5-29%)
Hemodialysis-associated amyloidosis
Very rare (1-4%)
Hereditary hemochromatosis
Wiskott-Aldrich syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 361135004
- UMLS CUI
- C1744601
- Fully Specified Name
- Abnormal cardiac rate (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.