Overview
Unable to walk is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Killian-Teschler-Nicola syndrome
Frequent (30-79%)
Friedreich's ataxia
Occasional (5-29%)
Adenylosuccinate lyase deficiency
Cockayne syndrome
Occasional (5-29%)
Glutaric aciduria, type 2
Very rare (1-4%)
Arachnoid cyst
Occasional (5-29%)
X-linked centronuclear myopathy
Occasional (5-29%)
Niemann-Pick disease, type A
Always present (100%)
Huntington's chorea
Occasional (5-29%)
Pelizaeus-Merzbacher disease
Always present (100%)
Ataxia-telangiectasia syndrome
Frequent (30-79%)
Rett's disorder
Occasional (5-29%)
I-cell disease
Frequent (30-79%)
Angelman syndrome
Occasional (5-29%)
Dihydrouracil dehydrogenase (NADP^+^) deficiency
Occasional (5-29%)
Steinert myotonic dystrophy syndrome
Very rare (1-4%)
Dyggve-Melchior-Clausen syndrome
Occasional (5-29%)
Salla disease
Tay-Sachs disease
Occasional (5-29%)
Chediak-Higashi syndrome
Occasional (5-29%)
Merosin deficient congenital muscular dystrophy
Very frequent (80-99%)
Aicardi Goutieres syndrome
Always present (100%)
Lafora disease
Frequent (30-79%)
Autosomal dominant sensory neuropathy
Occasional (5-29%)
Lobar holoprosencephaly
Very rare (1-4%)
Quick Facts
- SNOMED CT
- 282145008
- UMLS CUI
- C0560046
- Fully Specified Name
- Unable to walk (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.