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.
Dubowitz's syndrome
Occasional (5-29%)
Agenesis of corpus callosum
Occasional (5-29%)
Bardet-Biedl syndrome
Frequent (30-79%)
Ring chromosome 20 syndrome
Occasional (5-29%)
Metachromatic leukodystrophy, adult type
Frequent (30-79%)
Chorea acanthocytosis syndrome
Occasional (5-29%)
Multiple endocrine neoplasia, type 1
Occasional (5-29%)
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
Frequent (30-79%)
Metachromatic leukodystrophy, juvenile type
Frequent (30-79%)
Rubinstein-Taybi syndrome
Infantile neuroaxonal dystrophy
Occasional (5-29%)
Hyperlysinemia
Frequent (30-79%)
Mannosidosis, type I
Frequent (30-79%)
Swanson-Buchanan-Alvord neuropathy syndrome
Occasional (5-29%)
Cholestanol storage disease
Occasional (5-29%)
Williams syndrome
Frequent (30-79%)
5p partial monosomy syndrome
Steinert myotonic dystrophy syndrome
Occasional (5-29%)
Opitz-Frias syndrome
Frequent (30-79%)
Shwachman syndrome
Occasional (5-29%)
Tay-Sachs disease
Frequent (30-79%)
Deficiency of pyrroline-5-carboxylate reductase
Occasional (5-29%)
Phenylketonuria
Occasional (5-29%)
Dravet syndrome
Occasional (5-29%)
Landau-Kleffner syndrome
Occasional (5-29%)
Related Symptoms
Quick Facts
- SNOMED CT
- 247762003
- UMLS CUI
- C0262630
- Fully Specified Name
- Reduced concentration span (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.