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.
Cross syndrome
Occasional (5-29%)
Megaloblastic anemia due to impaired absorption of folate
Leigh's disease
Occasional (5-29%)
Paroxysmal choreoathetosis
Very frequent (80-99%)
Niemann-Pick disease, type A
Cutis laxa-corneal clouding-oligophrenia syndrome
Very frequent (80-99%)
Congenital defect of folate absorption
Salla disease
Pelizaeus-Merzbacher disease, classic form
Frequent (30-79%)
Pyruvate carboxylase deficiency
Occasional (5-29%)
Deficiency of guanidinoacetate methyltransferase
Occasional (5-29%)
Deficiency of tryptophan decarboxylase
Always present (100%)
3-Methylglutaconic aciduria type 1
Occasional (5-29%)
Congenital methemoglobinemia
Occasional (5-29%)
Glutaryl-CoA dehydrogenase deficiency
Frequent (30-79%)
Paroxysmal kinesigenic choreoathetosis
Very frequent (80-99%)
X-linked creatine deficiency syndrome
Frequent (30-79%)
Monocarboxylate transporter 8 deficiency
FOXG1 syndrome
Infantile leukoencephalopathy and megalencephaly
Occasional (5-29%)
Cystic leukoencephalopathy without megalencephaly
Occasional (5-29%)
Infantile onset spinocerebellar ataxia
Always present (100%)
TARP syndrome
Frequent (30-79%)
Autosomal recessive limb girdle muscular dystrophy type 2S
Autosomal recessive spastic paraplegia type 21
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 58593005
- UMLS CUI
- C0004158
- Fully Specified Name
- Athetoid movement (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.