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 neoplasm (MONDO:0005165)
Parent Node: urinary system neoplasm (MONDO:0021066)
..Starting node ..benign urinary system neoplasm ()
Child Nodes:
........benign prostate phyllodes tumor ()
........benign urethral neoplasm ()
........bladder benign neoplasm ()
........kidney benign neoplasm ()
........ureter benign neoplasm ()
........urothelial papilloma ()
Sister Nodes:
..benign urinary system neoplasm ()
..kidney neoplasm ()
..malignant urinary system neoplasm ()
..prostate phyllodes tumor ()
..ureter neoplasm ()
..urethra neoplasm ()
..urinary bladder neoplasm ()
..urothelial neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4180
Name:	benign urinary system neoplasm
Definition:	A non-metastasizing neoplasm that arises from the organs that comprise the urinary system. Representative examples include renal oncocytoma, bladder inverted papilloma, and urothelial papilloma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign neoplasm of the urinary tract; benign neoplasm of urinary tract; benign tumor of the urinary tract; benign tumor of urinary tract; benign urinary system neoplasm; benign urinary tract neoplasm; benign urinary tract tumor; neoplasm of urinary system; renal system benign neoplasm; tumor of the
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: FANCD2;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal