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Pure hereditary spastic paraplegia
ORPHA:102012
Classification level: Group of disorders- Synonym(s):
- Pure HSP
- Pure SPG
- Pure familial spastic paraplegia
- Uncomplicated HSP
- Uncomplicated SPG
- Uncomplicated familial spastic paraplegia
- Uncomplicated hereditary spastic paraplegia
- Prevalence: -
- Inheritance: -
- Age of onset: -
- ICD-10: G11.4
- OMIM: -
- UMLS: C0393555
- MeSH: -
- GARD: -
- MedDRA: -
Summary
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
Detailed information
Article for general public
Professionals
- Anesthesia guidelines
- Français (2019, pdf)
- Clinical genetics review
- English (2018)
- Disability factsheet
- Dansk (2018)
- Français (2018, pdf)
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.