Diastematomyelia

Preferred Label : Diastematomyelia;

NCIt definition : A rare congenital abnormality in which the spinal cord is split in half by fibrous or bony tissue. It may present as an isolated phenomenon or in association with spina bifida.;

Details

Origin ID

C98913;

UMLS CUI

C0011999;

Automatic exact mappings (from CISMeF team)
- Diastematomyelia [ACR pathology]
- Diastematomyelia [ICD-9 code]
- Split spinal cord malformation (disorder) [SNOMED CT concept]
- neural tube defects [MeSH Descriptor]
Currated CISMeF NLP mapping
- Diastematomyelia [ICD-10 Sub-category]
- Diastematomyelia [ICD-10 Sub-category (who)]
- Diastematomyelia [HRDO Sign]
- Diastematomyelia [PASCAL descriptor]
- Diastematomyelia [MedDRA Preferred Term]
- Diastematomyelia [OMIM Phenotype]
- Diastematomyelia [ICD-11 Subcategory]
- Diastematomyelia (disorder) [Inactive SNOMED CT concept]
- Split cord malformation type I [ORDO Disease]
- diastematomyelia [SNOMED Notion]
- diastematomyelia [Disease (Nov.)]
- diastematomyelia [MeSH concept]
Has associated anatomic sites
- Nervous System [NCIt concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Diastematomyelia [MedDRA Preferred Term]
- Diastematomyelia [ICD-10 Sub-category (who)]
- Diastematomyelia [OMIM Phenotype]
- Diastematomyelia [ICD-10 Sub-category]
- Diastematomyelia [HRDO Sign]
- Diastematomyelia [PASCAL descriptor]
- Diastematomyelia [ICD-9 code]
- Diastematomyelia [ICD-11 Subcategory]
- Diastematomyelia (disorder) [Inactive SNOMED CT concept]
- Split cord malformation type I [ORDO Disease]
- Split spinal cord malformation (disorder) [SNOMED CT concept]
- diastematomyelia [SNOMED Notion]
- diastematomyelia [MeSH concept]
- diastematomyelia [Disease (Nov.)]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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