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
Occasional (5-29%)
Listeriosis
Occasional (5-29%)
Typhoid fever
Occasional (5-29%)
Hypertyrosinemia, Richner-Hanhart type
Occasional (5-29%)
Crigler-Najjar syndrome, type I
Occasional (5-29%)
Cystathioninuria
Occasional (5-29%)
Neuroleptic malignant syndrome
Frequent (30-79%)
Corticobasal degeneration
Frequent (30-79%)
GTP cyclohydrolase I deficiency
Always present (100%)
Kearns-Sayre syndrome
Occasional (5-29%)
African trypanosomiasis
Occasional (5-29%)
Cocaine intoxication
Very rare (1-4%)
Orthostatic hypotension
Progressive supranuclear ophthalmoplegia
Occasional (5-29%)
Dihydrolipoamide dehydrogenase deficiency
Always present (100%)
Thyrotoxic periodic paralysis
Frequent (30-79%)
Hypogonadotropic hypogonadism
Occasional (5-29%)
Trisomy X syndrome
Occasional (5-29%)
Xeroderma pigmentosum, group G
Occasional (5-29%)
Hereditary acrodermatitis enteropathica
XXXXY syndrome
Occasional (5-29%)
Argininosuccinate lyase deficiency
Occasional (5-29%)
Globoid cell leukodystrophy, late-onset
Occasional (5-29%)
Xeroderma pigmentosum, group F
Occasional (5-29%)
Metachromatic leukodystrophy, juvenile type
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 26079004
- UMLS CUI
- C0040822
- Fully Specified Name
- Tremor (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.