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Autosomal recessive hereditary spastic paraplegia

disorder
SNOMED 1187279003CUI C0751603

Overview

Autosomal recessive hereditary spastic paraplegia is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Infantile-onset ascending hereditary spastic paralysis(child)
Autosomal recessive spastic paraplegia type 58(child)
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Autosomal recessive spastic paraplegia type 35(child)
Autosomal recessive spastic paraplegia type 21(child)
Autosomal recessive spastic paraplegia type 43(child)
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Autosomal recessive spastic paraplegia type 45(child)
Autosomal recessive spastic paraplegia type 67(child)
Autosomal recessive spastic paraplegia type 59(child)
SPOAN and SPOAN-related disorder(child)
Hereditary sensory and autonomic neuropathy with spastic paraplegia(child)
Autosomal recessive spastic paraplegia type 39(child)
Autosomal recessive spastic paraplegia type 44(child)
Autosomal recessive spastic paraplegia type 46(child)
Autosomal recessive spastic paraplegia type 53(child)

Quick Facts

SNOMED CT
1187279003
UMLS CUI
C0751603
Fully Specified Name
Autosomal recessive hereditary spastic paraplegia (disorder)
Specialists
0
Diagnostic Biomarkers
0
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.