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 urinary system neoplasm (MONDO:0004180)
Parent Node: ureter neoplasm (MONDO:0021111)
..Starting node ..ureter benign neoplasm ()
Child Nodes:
........schwannoma of ureter ()
........ureter leiomyoma ()
........ureter urothelial papilloma ()
Sister Nodes:
..polyp of ureter ()
..ureter benign neoplasm ()
..ureter cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1398
Name:	ureter benign neoplasm
Definition:	Cancer or tumors of the ureter which may cause obstruction leading to hydroureter, hydronephrosis, and pyelonephritis. hematuria is a common symptom.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign neoplasm of the ureter; benign neoplasm of ureter; benign tumor of the ureter; benign tumor of ureter; benign ureter neoplasm; benign ureter tumor; benign ureteral neoplasm; benign ureteral tumor; benign ureteric neoplasm; benign ureteric neoplasm NOS; neoplasm of ureter; ureter benign neopla
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal