Childhood Gliomatosis Cerebri

Preferred Label : Childhood Gliomatosis Cerebri;

NCIt related terms : Gliomatosis Cerebri;

Alternative definition : NICHD: Gliomatosis cerebri that occurs during childhood.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL433930;

Details

Origin ID

C114969;

UMLS CUI

C3897070;

Automatic exact mappings (from CISMeF team)
- Gliomatosis cerebri [ICD-11 Extension code]
- Gliomatosis cerebri [ICD-11 Extension code]
- Gliomatosis cerebri [MedDRA Preferred Term]
- Gliomatosis cerebri [ICD-O code]
- Gliomatosis cerebri [ICD-9 code]
- Gliomatosis cerebri (morphologic abnormality) [SNOMED CT concept]
- gliomatosis cerebri [DO Concept]
- gliomatosis cerebri [Radlex concept]
- gliomatosis cerebri [MeSH concept]
- gliomatosis cerebri [SNOMED Notion]
- neoplasms, neuroepithelial [MeSH Descriptor]
Disease may have findings
- Headache [NCIt concept]
- Papilledema [NCIt concept]
- Seizure [NCIt concept]
- Sensory Manifestations [NCIt concept]
- Unfavorable Clinical Outcome [NCIt concept]
Excludes anatomical site(s)
- Spinal Cord [NCIt concept]
Has associated anatomic sites
- Brain [NCIt concept]
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
Validated automatic mappings to NTBT
- Gliomatosis cerebri [ORDO Disease]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Elongated Glial Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Diffuse Pattern [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_primary_anatomic_site
- Brain [NCIt concept]
- Central Nervous System [NCIt concept]
- Cerebral Hemisphere [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 21 [NCIt concept]
- del(14q21) [NCIt concept]
- del(19p12) [NCIt concept]
- del(6q25) [NCIt concept]
- der(15;21)(q10;q10) [NCIt concept]

Keyword's position in hierarchy(ies) :

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