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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: Neurologic Manifestations (D009461)
Parent Node: Urinary Bladder Diseases (D001745)
..Starting node ..Urinary Bladder, Neurogenic (D001750)
Child Nodes:
Sister 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
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11416
Name:	Urinary Bladder, Neurogenic
Definition:	Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES.
Alternative IDs:
ParentIDs:	MESH:D001745\|MESH:D009461
TreeNumbers:	C10.597.900 \|C12.777.829.839 \|C13.351.968.829.760 \|C23.888.592.900
Synonyms:	Atonic Neurogenic Bladder \|Bladder Disorder, Neurogenic \|Bladder Neurogenesis \|Bladder, Neurogenic \|Neurogenesis, Bladder \|Neurogenesis, Urinary Bladder \|Neurogenic Bladder \|Neurogenic Bladder, Atonic \|Neurogenic Bladder Disorder \|Neurogenic Bladder Disorders \|Neu
Slim Mappings:	Nervous system disease\|Signs and symptoms\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D001750 MeSH: D001750 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants