01
ABCD1
No data
Diseases
Spastic Paraplegia, Hereditary
spastic paraplegia, hereditary
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
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Core Information
- Disease Name
- Spastic Paraplegia, Hereditary
- Standard Disease Name
- spastic paraplegia, hereditary
- MeSH Tree
- No data
- ICD-10
- G11.4
Identifiers
- DO ID
- No data
- MeSH ID
- D015419
- OMIM ID
- 600361
- UMLS ID
- C0037773
- HPO ID
- No data
Description and Extensions
- Description
- MSH2017_2016_08_12:A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8)
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