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Metadata
ID DOID:0080684
PURL http://purl.obolibrary.org/obo/DOID_0080684 Copy
Name diffuse midline glioma, H3 K27-altered
Definition A histone mutated tumor that is characterized by loss of histone H3 p.K28me3 (K27me3) methylation and located throughout the midline structures of the central nervous system. Methylation loss may be due to p.K28M (K27M) mutation in one of the histone H3 isoforms (H3.1, H3.2, or H3.3), overexpression of EZHIP, or mutation of the EGFR gene.
https://pubmed.ncbi.nlm.nih.gov/30800634/, https://pmc.ncbi.nlm.nih.gov/articles/PMC9763979/, https://pmc.ncbi.nlm.nih.gov/articles/PMC8328013/, https://pubmed.ncbi.nlm.nih.gov/31290035/
Xrefs

GARD:0026785

ICD10CM:C71.9

ICDO:9385/3

NCI:C185368

ORDO:723358

UMLS_CUI:C5669877

SKOS

exactMatch ORDO:723358

exactMatch UMLS_CUI:C5669877

exactMatch ICDO:9385/3

exactMatch NCI:C185368

narrowMatch GARD:0026785

broadMatch ICD10CM:C71.9

Subsets

DO_cancer_slim

NCIthesaurus

Synonyms

diffuse intrinsic pontine glioma [EXACT]

diffuse midline glioma, H3 K27M-mutant [EXACT]

Parent Relationships

is_a histone mutated tumor

Subclass Logical Relationships

derives from some glial cell

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