Astroblastoma, MN1-Altered

Preferred Label : Astroblastoma, MN1-Altered;

NCIt related terms : Astroblastoma;

NCIt definition : A rare glial neoplasm characterized by structural rearrangements of the MN1 gene at chromosome band 22q12.1. It is usually found in the cerebral hemispheres of young adults and children and predominantly affects females. Morphologically, it consists of elongated glial cells with abundant eosinophilic cytoplasm and GFAP-positive processes, arranged perivascularly.;

Neoplastic status : Undetermined;

ICD-O code : 9430/3;

Details

Origin ID

C4324;

UMLS CUI

C0334587;

Automatic exact mappings (from CISMeF team)
- Astroblastoma [ICD-11 Extension code]
- Astroblastoma [MedDRA Preferred Term]
- astroblastoma, MN1-altered [DO Concept]
Currated CISMeF NLP mapping
- Astroblastoma [ICD-9 code]
- Astroblastoma [ICD-O code]
- Astroblastoma [ORDO Disease]
- Astroblastoma (morphologic abnormality) [SNOMED CT concept]
- astroblastoma [DO Concept]
- astroblastoma [Disease (Nov.)]
- astroblastoma [MeSH concept]
- astroblastoma [SNOMED Notion]
- astroblastoma [Radlex concept]
- neoplasms, neuroepithelial [MeSH Descriptor]
DO Cross reference
- astroblastoma [DO Concept]
Disease may have findings
- Necrotic Change [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Astroblastoma [ICD-O code]
- Astroblastoma [ICD-9 code]
- Astroblastoma [ORDO Disease]
- Astroblastoma [MedDRA Preferred Term]
- Astroblastoma (morphologic abnormality) [SNOMED CT concept]
- astroblastoma [DO Concept]
- astroblastoma [Disease (Nov.)]
- astroblastoma [MeSH concept]
- astroblastoma [SNOMED Notion]
concept_is_in_subset
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology Terminology [NCIt concept]
- Mapped ICDO3.1 Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 Terminology [NCIt concept]
- NCIt Neoplasm Core Terminology [NCIt concept]
disease_excludes_finding
- Precise Histogenesis Unknown [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Glial Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell and Neoplastic Perineural Cell [NCIt concept]
disease_has_finding
- Perivascular Pseudorosette Formation [NCIt concept]
disease_has_molecular_abnormality
- MN1 Gene Rearrangement [NCIt concept]
disease_has_normal_cell_origin
- Glial Cell [NCIt concept]
- Neuroepithelial Cell [NCIt concept]
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
disease_has_normal_tissue_origin
- Nerve Tissue, Neuroepithelial Tissue, and Nerve Sheaths [NCIt concept]
- Neuroepithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
disease_mapped_to_gene
- MN1 Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Monosomy 10 [NCIt concept]
- Monosomy 21 [NCIt concept]
- Monosomy 22 [NCIt concept]
pathogenesis_of_disease_involves_gene
- MN1 Gene [NCIt concept]
- MN1 wt Allele [NCIt concept]

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