MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: kidney disease (MONDO:0005240)
Parent Node: urinary system neoplasm (MONDO:0021066)
..Starting node ..kidney neoplasm ()
Child Nodes:
........childhood kidney neoplasm ()
........inherited renal tumor ()
........kidney benign neoplasm ()
........kidney cancer ()
........kidney hemangiopericytoma ()
........mesonephric neoplasm ()
........mixed epithelial stromal tumor of the kidney ()
........multiloculated renal cyst ()
........non-amyloid monoclonal immunoglobulin deposition disease ()
........renal pelvis neoplasm ()
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:	21163
Name:	kidney neoplasm
Definition:	A benign or malignant neoplasm affecting the kidney. Representative examples of benign renal neoplasms include fibroma, lipoma, oncocytoma, and juxtaglomerular cell tumor. Representative examples of malignant renal neoplasms include renal cell carcinoma, renal pelvis carcinoma, Wilms tumor, rhabdoid tumor, sarcoma, and lymphoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	kidney neoplasm; kidney neoplasm (disease); kidney tumor; neoplasm of kidney; neoplasm of the kidney; renal neoplasm; renal tumor; renal tumors; tumor of kidney; tumor of the kidney
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal