Hereditary Spastic Paraplegia

Preferred Label : Hereditary Spastic Paraplegia;

NCIt definition : Spastic paraplegia that is transmitted from parent to child.;

Codes from synonyms : G11.4;

Details

Origin ID

C140267;

UMLS CUI

C0037773;

Currated CISMeF NLP mapping
- Hereditary spastic paraplegia [ICD-10 Sub-category]
- Hereditary spastic paraplegia [ORDO Disease]
- Hereditary spastic paraplegia [PASCAL descriptor]
- Hereditary spastic paraplegia [MedDRA Preferred Term]
- Hereditary spastic paraplegia [ICD-11 Subcategory]
- Hereditary spastic paraplegia [ICD-9 code]
- Hereditary spastic paraplegia [ICD-10 Sub-category (who)]
- Hereditary spastic paraplegia (disorder) [SNOMED CT concept]
- X-linked hereditary spastic paraplegia [ICD-11 Sub-sub category]
- hereditary sensory-motor neuropathy, type v [SNOMED Notion]
- hereditary spastic paraplegia [SNOMED Notion]
- hereditary spastic paraplegia [DO Concept]
- hereditary spastic paraplegia [Disease (Nov.)]
- spastic paraplegia, hereditary [MeSH Descriptor]
- spastic paraplegia, hereditary [MeSH concept]
DO Cross reference
- hereditary spastic paraplegia [DO Concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary motor and sensory neuropathy V [OMIM Phenotype]
- Hereditary motor and sensory neuropathy type 5 [ORDO Disease]
- Hereditary sensory-motor neuropathy, type V (disorder) [SNOMED CT concept]
- Hereditary spastic paraplegia [ICD-10 Sub-category]
- Hereditary spastic paraplegia [ICD-9 code]
- Hereditary spastic paraplegia [MedDRA Preferred Term]
- Hereditary spastic paraplegia [ICD-11 Subcategory]
- Hereditary spastic paraplegia (disorder) [SNOMED CT concept]
- X-linked hereditary spastic paraplegia [ICD-11 Sub-sub category]
- hereditary sensory-motor neuropathy, type v [SNOMED Notion]
- hereditary spastic paraplegia [SNOMED Notion]
- hereditary spastic paraplegia [DO Concept]
- spastic paraplegia, hereditary [MeSH Descriptor]
- spastic paraplegia, hereditary [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- mCode Elixhauser Neurological Movement Disorder Value Set [NCIt concept]
- mCode Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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