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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: Pinealoma (D010871)
Parent Node: Teratoma (D013724)
..Starting node ..Pineal Teratoma (C537401)
Child Nodes:
Sister Nodes:
..Dermoid Cyst (D003884) 5
..Malignant Teratocarcinosarcoma (C535701)
..Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia (C538340)
..Pineal Teratoma (C537401)
..Sacral Agenesis Syndrome (C566762)
..Struma Ovarii (D013330)
..Teratoid Tumor, Atypical (C563737)
..Teratoma, Ovarian (C562731)
..Teratoma, Testicular (C562472)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8947
Name:	Pineal Teratoma
Definition:
Alternative IDs:
ParentIDs:	MESH:D010871\|MESH:D013724
TreeNumbers:	C04.557.465.625.600.657/C537401 \|C04.557.465.910/C537401 \|C04.557.470.670.657/C537401 \|C04.557.580.625.600.657/C537401 \|C04.588.614.250.195.766/C537401 \|C10.228.140.211.788/C537401 \|C10.551.240.250.625/C537401
Synonyms:	Teratoma, Pineal
Slim Mappings:	Cancer\|Nervous system disease
Reference:	MedGen: C537401 MeSH: C537401 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants