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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: Lipomatosis (D008068)
Parent Node: Urinary Bladder Diseases (D001745)
..Starting node ..Pelvic lipomatosis (C535549)
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:	8755
Name:	Pelvic lipomatosis
Definition:
Alternative IDs:
ParentIDs:	MESH:D001745\|MESH:D008068
TreeNumbers:	C12.777.829/C535549 \|C13.351.968.829/C535549 \|C17.800.463/C535549 \|C18.452.584.718/C535549
Synonyms:
Slim Mappings:	Metabolic disease\|Skin disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C535549 MeSH: C535549 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants