Childhood infratentorial neoplasm

Summary

Childhood infratentorial neoplasm (MONDO:0002915) is a cancer. A subtype of childhood neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	childhood infratentorial neoplasm
Mondo ID	MONDO:0002915
DOID	DOID:4207
NCIT	C5802
UMLS	C1332973
MedGen	232349
Is cancer (heuristic)	yes

Also known as: childhood infratentorial neoplasm · childhood infratentorial neoplasms · childhood infratentorial tumor · childhood infratentorial tumors · childhood infratentorial tumour · childhood infratentorial tumours · infratentorial neoplasm of childhood · paediatric infratentorial neoplasm · paediatric infratentorial tumour · pediatric infratentorial neoplasm · pediatric infratentorial tumor

Disease family

This is a subtype of childhood neoplasm. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › childhood neoplasm › childhood infratentorial neoplasm

Related subtypes (13): childhood astrocytic tumor, childhood spinal cord tumor, childhood kidney neoplasm, pediatric meningioma, childhood mediastinal neurogenic neoplasm, childhood ependymoma, childhood germ cell tumor, childhood optic nerve glioma, childhood malignant neoplasm, childhood carcinoid tumor, childhood choroid plexus neoplasm, childhood testicular neoplasm, childhood adrenal gland pheochromocytoma

Subtypes (4): childhood brain stem neoplasm, childhood cerebellar neoplasm, pediatric infratentorial ependymoma, pediatric infratentorial ependymoblastoma

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.