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
Very rare (1-4%)
Friedreich's ataxia
Frequent (30-79%)
Cockayne syndrome
Occasional (5-29%)
Metachromatic leukodystrophy, adult type
Occasional (5-29%)
Glutathione synthase deficiency with 5-oxoprolinuria
Metachromatic leukodystrophy, juvenile type
Occasional (5-29%)
Roussy-Lévy syndrome
Cowden syndrome
Urocanate hydratase deficiency
Very frequent (80-99%)
Pelizaeus-Merzbacher disease
Always present (100%)
Niemann-Pick disease, type C
Occasional (5-29%)
Lhermitte-Duclos disease
Dentatorubropallidoluysian degeneration
Frequent (30-79%)
Ataxia-telangiectasia syndrome
Frequent (30-79%)
Gamma-glutamyl transpeptidase deficiency
Frequent (30-79%)
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
Frequent (30-79%)
Deficiency of uridyl transferase
Frequent (30-79%)
Unverricht-Lundborg syndrome
Frequent (30-79%)
Dravet syndrome
Occasional (5-29%)
Neonatal pseudo-hydrocephalic progeroid syndrome
Multiple symmetrical lipomatosis
Occasional (5-29%)
Carbohydrate-deficient glycoprotein syndrome type I
Frequent (30-79%)
Deficiency of UTP-hexose-1-phosphate uridylyltransferase
Frequent (30-79%)
Medulloblastoma
Frequent (30-79%)
Fragile X associated tremor ataxia syndrome
Quick Facts
- SNOMED CT
- 30721006
- UMLS CUI
- C4551520
- Fully Specified Name
- Intention 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.