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.
Friedreich's ataxia
Frequent (30-79%)
Renal carnitine transport defect
Very frequent (80-99%)
Metachromatic leukodystrophy, adult type
Frequent (30-79%)
Metachromatic leukodystrophy, congenital type
Frequent (30-79%)
Globoid cell leukodystrophy, late-onset
Frequent (30-79%)
Metachromatic leukodystrophy, juvenile type
Frequent (30-79%)
Roussy-Lévy syndrome
Frequent (30-79%)
Metachromatic leukodystrophy, late infantile type
Frequent (30-79%)
Retinitis pigmentosa-deafness syndrome
Occasional (5-29%)
Congenital myotonia, autosomal dominant form
Occasional (5-29%)
Hyperlysinemia
Occasional (5-29%)
Huntington's chorea
Frequent (30-79%)
Distal muscular dystrophy
Frequent (30-79%)
Mannosidosis, type I
Occasional (5-29%)
Adrenoleukodystrophy
Very frequent (80-99%)
Niemann-Pick disease, type C
Occasional (5-29%)
Angelman syndrome
Very frequent (80-99%)
Wilson's disease
Very frequent (80-99%)
Isolated thyrotropin deficiency
Occasional (5-29%)
Oromandibular-limb hypogenesis spectrum
Azorean disease
Very frequent (80-99%)
Tay-Sachs disease
Frequent (30-79%)
Deficiency of uridyl transferase
Occasional (5-29%)
Galactosylceramide lipidosis
Occasional (5-29%)
Westphal-Strumpell syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 7006003
- UMLS CUI
- C0233844
- Fully Specified Name
- Clumsiness (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.