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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: Lipoma (D008067)
..Starting node ..Lipoblastoma (D062689)
Child Nodes:
Sister Nodes:
..Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi (C567863)
..Lipoblastoma (D062689)
..Lipoma of the Conjunctiva (C563620)
..LIPOMATOSIS, MULTIPLE (OMIM:151900)
..Lipomatous hemangiopericytoma (C537029)
..Median cleft lip, corpus callosum, lipoma, and skin polyps (C536135)
..Nasopalpebral lipoma coloboma syndrome (C538338)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6464
Name:	Lipoblastoma
Definition:	Benign tumors of fatty tissues found in infancy and childhood. It is associated chromosomal aberrations that result in activation of an oncogene on chromosome band 8q12.
Alternative IDs:
ParentIDs:	MESH:D008067
TreeNumbers:	C04.557.450.550.400.500
Synonyms:	Lipoblastomas \|Lipoblastomatoses \|Lipoblastomatosis
Slim Mappings:	Cancer
Reference:	MedGen: D062689 MeSH: D062689 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants