Disease browser and phenotype portal

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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: Nervous System Neoplasms (D009423)
..Starting node ..Central Nervous System Neoplasms (D016543)
Child Nodes:
........Brain Neoplasms (D001932) 30
........Central Nervous System Cysts (D020863) 11
........Meningeal Neoplasms (D008577) 5
........Spinal Cord Neoplasms (D013120) 1
Sister Nodes:
..Central Nervous System Neoplasms (D016543) 50
..Cranial Nerve Neoplasms (D003390) 4
..Melanoma astrocytoma syndrome (C536149)
..Paraneoplastic Syndromes, Nervous System (D020361) 10
..Peripheral Nervous System Neoplasms (D010524) 25
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1904
Name:	Central Nervous System Neoplasms
Definition:	Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges.
Alternative IDs:
ParentIDs:	MESH:D009423
TreeNumbers:	C04.588.614.250 \|C10.551.240
Synonyms:	Central Nervous System Neoplasms, Primary \|Central Nervous System Tumors \|Neoplasms, Central Nervous System \|Primary Central Nervous System Neoplasms \|Tumors, Central Nervous System
Slim Mappings:	Cancer\|Nervous system disease
Reference:	MedGen: D016543 MeSH: D016543 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants