MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation 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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: benign digestive system neoplasm (MONDO:0000385)
Parent Node: benign endocrine neoplasm (MONDO:0000627)
Parent Node: intra-abdominal hemangioma (MONDO:0002337)
Parent Node: liver neoplasm (MONDO:0004721)
..Starting node ..liver hemangioma ()
Child Nodes:
........liver cavernous hemangioma ()
Sister Nodes:
..biliary tract neoplasm (disease) ()
..hepatic angiomyolipoma ()
..hepatic granuloma ()
..hepatocellular adenoma ()
..liver cancer ()
..liver hemangioma ()
..liver inflammatory myofibroblastic tumor ()
..liver leiomyoma ()
..liver lipoma ()
..liver mesenchymal hamartoma ()
..liver solitary fibrous tumor ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2404
Name:	liver hemangioma
Definition:	A hemangioma arising from the liver.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	angioma of liver; angioma of the liver; hemangioma of liver; hemangioma of liver; hemangioma of the liver; hepatic angioma; hepatic hemangioma; liver angioma; liver hemangioma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal