spongy degeneration of central nervous system

Preferred Label : spongy degeneration of central nervous system;

Details

Origin ID

DA-20168;

UMLS CUI

C0206307;

Currated CISMeF NLP mapping
- Canavan Disease [NCIt concept]
- Canavan disease [MedDRA Preferred Term]
- Canavan disease [PASCAL descriptor]
- Canavan disease [Disease (Nov.)]
- Canavan disease [DO Concept]
- Canavan disease [ACR pathology]
- Canavan disease [ICD-11 More detail]
- Canavan disease [OMIM Phenotype]
- Canavan disease [ORDO Disease]
- Spongy degeneration of central nervous system (disorder) [SNOMED CT concept]
- aspartoacylase [ORDO Gene]
- canavan disease [MeSH Descriptor]
- canavan disease [MeSH concept]
ICD-10 exact mapping(s)
- Other sphingolipidosis [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Autosomal recessive syndromic optic atrophy [ORDO Disease]
- Cerebral organic aciduria [ORDO Disease]
- Disorder of amino acid and other organic acid metabolism [ORDO Disease]
- Genetic neurodegenerative disease [ORDO Disease]
- Neurometabolic disease [ORDO Disease]
- Rare neurodegenerative disease [ORDO Disease]
Metaterm(s)
- neurology [CISMeF Metaterm]
SNOMED CT concept
- Spongy degeneration of central nervous system (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Canavan Disease [NCIt concept]
- Canavan disease [MedDRA Preferred Term]
- Canavan disease [ORDO Disease]
- Canavan disease [OMIM Phenotype]
- Canavan disease [Disease (Nov.)]
- Canavan disease [DO Concept]
- Canavan disease [PASCAL descriptor]
- Canavan disease [ACR pathology]
- Canavan disease [ICD-11 More detail]
- Spongy degeneration of central nervous system (disorder) [SNOMED CT concept]
- aspartoacylase [ORDO Gene]
- canavan disease [MeSH Descriptor]
- canavan disease [MeSH concept]

Keyword's position in hierarchy(ies) :

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