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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

Disease Browser
Parent Node: Urologic Diseases (D014570)
..Starting node ..Urinary Bladder Diseases (D001745)
Child Nodes:
........Bladder Exstrophy (D001746) 1
........Cystitis (D003556) 2
........Cystocele (D052858)
........Panic Disorder with Bladder Conditions (C566834)
........Pelvic lipomatosis (C535549)
........Urinary Bladder Calculi (D001744)
........Urinary Bladder Fistula (D001747) 1
........Urinary Bladder Neck Obstruction (D001748)
........Urinary Bladder Neoplasms (D001749) 2
........Urinary Bladder, Neurogenic (D001750)
........Urinary Bladder, Overactive (D053201)
........Vesico-Ureteral Reflux (D014718) 5
Sister Nodes:
..Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities (C567716)
..Kidney Diseases (D007674) 345
..Ureteral Diseases (D014515) 6
..Urethral Diseases (D014522) 12
..Urinary Bladder Diseases (D001745) 23
..Urinary Tract Infections (D014552) 3
..Urination Disorders (D014555) 26
..Urofacial syndrome (C536480)
..Urolithiasis (D052878) 19
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11412
Name:	Urinary Bladder Diseases
Definition:	Pathological processes of the URINARY BLADDER.
Alternative IDs:
ParentIDs:	MESH:D014570
TreeNumbers:	C12.777.829 \|C13.351.968.829
Synonyms:	Bladder Disease \|Bladder Diseases \|Urinary Bladder Disease
Slim Mappings:	Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D001745 MeSH: D001745 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants