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 ..disease of genitourinary system ()
Child Nodes:
........autoimmune disease of urogenital tract ()
........familial vesicoureteral reflux ()
........inherited genitourinary tract anomalies (disease) ()
........multisystemic smooth muscle dysfunction syndrome ()
........reproductive system disease ()
........syndromic urogenital tract malformation ()
........urogenital neoplasm ()
........urogenital tuberculosis ()
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:	21145
Name:	disease of genitourinary system
Definition:	A disease that involves the genitourinary system.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	disease of genitourinary system; disease or disorder of genitourinary system; disorder of genitourinary system; disorder of genitourinary system; disorder of the genitourinary system; genitourinary system disease; genitourinary system disease or disorder; syndrome of the genitourinary system; urogen
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal