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| Term | hereditary spastic paraplegia | ID (Ontology) | DOID:2476 (Human Disease) | |||||||||||||||||||||||||||
| Definition | A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. | |||||||||||||||||||||||||||||
| Also Known As | "familial spastic paraplegia" ; "French settlement disease" ; "hereditary spastic paraparesis" (for all, see Synonyms field below) | |||||||||||||||||||||||||||||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Is a | paraplegia | ||
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:6637 ICD10CM:G11.4 ICD9CM:334.1 MESH:D015419 MIM:PS303350 NCI:C140267 SNOMEDCT_US_2023_03_01:267692008 UMLS_CUI:C0037773 |
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