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.
African trypanosomiasis
Occasional (5-29%)
Megaloblastic anemia due to impaired absorption of folate
Leigh's disease
Very rare (1-4%)
Paroxysmal choreoathetosis
Very frequent (80-99%)
Aspartylglucosaminuria
Very frequent (80-99%)
Pseudohypoparathyroidism type I B
Occasional (5-29%)
Congenital defect of folate absorption
Trypanosomiasis
Occasional (5-29%)
Marinesco-Sjogren syndrome
Frequent (30-79%)
Pyruvate carboxylase deficiency
Occasional (5-29%)
Deficiency of tryptophan decarboxylase
Occasional (5-29%)
Encephalitis lethargica
Frequent (30-79%)
Subacute sclerosing panencephalitis
Occasional (5-29%)
Early infantile epileptic encephalopathy with suppression bursts
Occasional (5-29%)
Blood group deletion syndrome
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Hereditary nonpolyposis colon cancer
Occasional (5-29%)
Van Bogaert's sclerosing leukoencephalitis
Occasional (5-29%)
Sulfite oxidase deficiency
Always present (100%)
Measles inclusion body encephalitis
Occasional (5-29%)
Mount-Reback syndrome
Occasional (5-29%)
Paroxysmal kinesigenic choreoathetosis
Very frequent (80-99%)
Adult onset basal ganglia disease
Monocarboxylate transporter 8 deficiency
Very rare (1-4%)
FOXG1 syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 9748009
- UMLS CUI
- C0013384
- Fully Specified Name
- Dyskinesia (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.