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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)
Parent Node: Neoplasms, Neuroepithelial (D018302)
..Starting node ..Pinealoma (D010871)
Child Nodes:
........Pineal Teratoma (C537401)
Sister Nodes:
..Ganglioneuroma (D005729) 1
..Glioma (D005910) 15
..Neurocytoma (D018306)
..Neuroectodermal Tumors, Primitive (D018242) 6
..Pinealoma (D010871) 1
..Retinoblastoma (D012175) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8946
Name:	Pinealoma
Definition:	Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670)
Alternative IDs:
ParentIDs:	MESH:D001932\|MESH:D018302
TreeNumbers:	C04.557.465.625.600.657 \|C04.557.470.670.657 \|C04.557.580.625.600.657 \|C04.588.614.250.195.766 \|C10.228.140.211.788 \|C10.551.240.250.625
Synonyms:	Mixed Pineocytoma Pineoblastoma \|Mixed Pineocytoma-Pineoblastoma \|Mixed Pineocytoma-Pineoblastomas \|Neoplasm, Pineal \|Neoplasms, Pineal \|Pineal Gland Tumor \|Pineal Gland Tumors \|Pineal Neoplasm \|Pineal Neoplasms \|Pinealocytoma \|Pinealocytomas \|Pinealomas \|Pineal Par
Slim Mappings:	Cancer\|Nervous system disease
Reference:	MedGen: D010871 MeSH: D010871 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants