Spastic pseudosclerosis

Preferred Label : Spastic pseudosclerosis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Disseminated encephalomyelopathy; CORTICOPALLIDODEGENERATION;

Inheritance : Autosomal recessive;

Prefixed ID : 270900;

Details

Origin ID

270900;

UMLS CUI

C0599464;

Currated CISMeF NLP mapping
- CREUTZFELDT-JAKOB DISEASE [WHO-ART Preferred Term]
- Creutzfeldt Jakob disease [Disease (Nov.)]
- Creutzfeldt-Jakob Disease [NCIt concept]
- Creutzfeldt-Jakob disease [PASCAL descriptor]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category]
- Creutzfeldt-Jakob disease [MedDRA Preferred Term]
- Creutzfeldt-Jakob disease [DO Concept]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category (who)]
- Creutzfeldt-Jakob syndrome [MeSH concept]
- Jakob-Creutzfeldt disease [MedDRA LLT]
- Jakob-Creutzfeldt disease (disorder) [SNOMED CT concept]
- Sporadic Creutzfeldt-Jakob disease [ORDO Disease]
- creutzfeldt-jakob disease [MedlinePlus Topic]
- creutzfeldt-jakob syndrome [MeSH Descriptor]
- jakob-creutzfeldt disease [SNOMED Notion]
- spastic pseudosclerosis [MeSH concept]
- spastic pseudosclerosis [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the nervous system [HPO term]
- Autosomal recessive inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- spastic pseudosclerosis [MeSH Supplementary Concept]
- spastic pseudosclerosis [MeSH concept]

Keyword's position in hierarchy(ies) :

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