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.
Cobalamin C disease
Occasional (5-29%)
Hereditary diffuse leukoencephalopathy with axonal spheroids
Always present (100%)
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
Frequent (30-79%)
Navajo neuropathy
Frequent (30-79%)
Spastic paraparesis, cataracts, speech delay syndrome
Occasional (5-29%)
Related Symptoms
Quick Facts
- SNOMED CT
- 736317001
- UMLS CUI
- C4544271
- Fully Specified Name
- Impaired executive functioning (finding)
- Associated Conditions
- 5
- 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.