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%)
Gilles de la Tourette's syndrome
Classical phenylketonuria
Coffin-Siris syndrome
Very rare (1-4%)
Trichotillomania
Chorea acanthocytosis syndrome
Occasional (5-29%)
De Lange syndrome
Frequent (30-79%)
Rheumatic chorea
Frequent (30-79%)
CHARGE association
Frequent (30-79%)
Huntington's chorea
Frequent (30-79%)
Williams syndrome
Frequent (30-79%)
Niemann-Pick disease, type C
Occasional (5-29%)
Lowe syndrome
Frequent (30-79%)
Pyruvate carboxylase deficiency
Occasional (5-29%)
Manganese pneumonitis
Frequent (30-79%)
Obsessive-compulsive disorder
Diurnal dystonia
Occasional (5-29%)
Blood group deletion syndrome
Leucocyte adhesion deficiency - type 2
Frequent (30-79%)
Maternal phenylketonuria
Floating-Harbor syndrome
Occasional (5-29%)
X-linked mental retardation with marfanoid habitus syndrome
Myoclonic dystonia
Frequent (30-79%)
Poisoning by manganese
Frequent (30-79%)
Fragile X associated tremor ataxia syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 12479006
- UMLS CUI
- C0600104
- Fully Specified Name
- Compulsive behavior (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.