disease has location cerebellar neoplasm embryonal neoplasm medulloblastoma https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/7005/medulloblastoma https://www.malacards.org/card/cerebellar_medulloblastoma https://www.malacards.org/card/medulloblastoma MONDO:0007959 MDB MESH:D008527 medulloblastoma, desmoplastic, autosomal recessive, autosomal dominant, somatic mutation ONCOTREE:MBL UMLS:C0025149 icd11.foundation:290815825 medulloblastomas medulloblastoma, malignant EFO:0002939 cerebellum embryonal neoplasm localised primitive neuroectodermal tumour SCTID:443333004 A malignant, invasive embryonal neoplasm arising from the cerebellum. It occurs predominantly in children and has the tendency to metastasize via the cerebrospinal fluid pathways. Signs and symptoms include truncal ataxia, disturbed gait, lethargy, headache, and vomiting. There are four histologic variants: classic medulloblastoma, large cell/anaplastic medulloblastoma, desmoplastic/nodular medulloblastoma, and medulloblastoma with extensive nodularity. MEDGEN:7517 DOID:0050902 NORD:1422 MedDRA:10027107 CPNET infratentorial primitive neuroectodermal tumour medulloblastoma, autosomal recessive, autosomal dominant, somatic mutation Orphanet:616 medulloblastoma, somatic DOID:0060104 ICDO:9470/3 OMIM:155255 medulloblastoma GARD:0007005 NANDO:2200090 NCIT:C3222 cerebellum