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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Brain Neoplasms (D001932)
..Starting node ..Cerebral Ventricle Neoplasms (D002551)
Child Nodes:
........Choroid Plexus Neoplasms (D016545) 2
Sister Nodes:
..Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert (C536367)
..Cerebral astrocytoma, adult (C535354)
..Cerebral sarcoma (C537946)
..Cerebral Ventricle Neoplasms (D002551) 3
..Cerebroretinal Microangiopathy with Calcifications and Cysts (C567401)
..Desmoplastic cerebral astrocytoma of infancy (C535945)
..Familial capillaro-venous leptomeningeal angiomatosis (C536609)
..Glioma of Brain, Familial (C564230)
..Infratentorial Neoplasms (D015192) 2
..Neurocytoma (D018306)
..Pascual Castroviejo syndrome (C536302)
..Pinealoma (D010871) 1
..PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY (OMIM:603688)
..Rhabdoid Tumor Predisposition Syndrome 1 (C563738)
..Supratentorial Neoplasms (D015173) 8
..Turcot syndrome (C536928)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1956
Name:	Cerebral Ventricle Neoplasms
Definition:	Neoplasms located in the brain ventricles, including the two lateral, the third, and the fourth ventricle. Ventricular tumors may be primary (e.g., CHOROID PLEXUS NEOPLASMS and GLIOMA, SUBEPENDYMAL), metastasize from distant organs, or occur as extensions of locally invasive tumors from adjacent brain structures.
Alternative IDs:
ParentIDs:	MESH:D001932
TreeNumbers:	C04.588.614.250.195.205 \|C10.228.140.211.280 \|C10.551.240.250.200
Synonyms:	Brain Ventricular Neoplasm \|Brain Ventricular Neoplasms \|Brain Ventricular Tumor \|Brain Ventricular Tumors \|Cerebral Ventricle Neoplasm \|Cerebral Ventricle Tumor \|Cerebral Ventricle Tumors \|Cerebroventricular Neoplasm \|Cerebroventricular Neoplasms \|Intraventricul
Slim Mappings:	Cancer\|Nervous system disease
Reference:	MedGen: D002551 MeSH: D002551 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants