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: gallbladder neoplasm (MONDO:0021253)
..Starting node ..benign neoplasm of gallbladder ()
Child Nodes:
........gallbladder leiomyoma ()
........gallbladder lipoma ()
Sister Nodes:
..benign neoplasm of gallbladder ()
..gallbladder biliary intraepithelial neoplasia ()
..gallbladder cancer ()
..gallbladder neuroendocrine neoplasm ()
..gallbladder papillary neoplasm ()
..polyp of gallbladder ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21503
Name:	benign neoplasm of gallbladder
Definition:	A benign neoplasm that involves the gall bladder.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign gallbladder neoplasm; benign gallbladder tumor; benign neoplasm of the gallbladder; benign tumor of gallbladder; benign tumor of the gallbladder; gall bladder benign neoplasm; gallbladder benign neoplasm; gallbladder benign tumor
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal