raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:715704

Infant-type hemispheric glioma MET-altered

Type
Etiological subtype
Group
Subtype of disorder
Inheritance
Not applicable
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enInfant-type hemispheric glioma MET-altered
frGliome hémisphérique infantile MET-altéré
deHemisphärisches Gliom vom infantilen Typ mit MET-Alteration
esGlioma hemisférico de tipo infantil con alteración de MET
itGlioma emisferico tipo infantile con alterazione di MET
nlInfantiel hemisferisch glioom MET-gewijzigd
ptInfant-type hemispheric glioma MET-altered
plGlejak półkulisty typu niemowlęcego ze zmianą MET
csInfant-type hemispheric glioma MET-altered
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

1 direct
GeneAssociationStatusHGNCEnsemblOMIMLocusNameSource of validation
METPart of a fusion gene inAssessedHGNC:7029ENSG000001059761648607q31.2MET proto-oncogene, receptor tyrosine kinase38902810[PMID]_31554817(PMID]
5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card