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: disease by anatomical system (MONDO:0021199)
..Starting node ..urinary system disease ()
Child Nodes:
........bacteriuria (disease) ()
........kidney disease ()
........pyuria (disease) ()
........Trichomonas vaginitis urogenital infection ()
........ureteral disease ()
........urethral disease ()
........urinary bladder disease ()
........urinary system neoplasm ()
........urinary tract infection (disease) ()
........urinary tract obstruction ()
........urolithiasis ()
........urothelial hyperplasia ()
Sister Nodes:
..cardiovascular disease ()
..digestive system disease ()
..disease of genitourinary system ()
..endocrine system disease ()
..hematologic disease ()
..immune system disease ()
..integumentary system disease ()
..mediastinal disease ()
..musculoskeletal system disease ()
..nervous system disorder ()
..respiratory system disease ()
..sensory system disease ()
..urinary system disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2118
Name:	urinary system disease
Definition:	A disease involving the renal system.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	disease of renal system; disease or disorder of renal system; disease, urinary tract; disease, urologic; disease, urological; diseases, urinary tract; diseases, urologic; diseases, urological; disorder of renal system; disorder of renal system; disorder of the urinary system; disorder of urinary sys
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal