Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Urination Disorders (D014555)
Parent Node: Urological Manifestations (D020924)
..Starting node ..Polyuria (D011141)
Child Nodes:
........Hyperphosphatemia, Polyuria, and Seizures (C565494)
Sister Nodes:
..Hypercalciuria (D053565) 6
..Lower Urinary Tract Symptoms (D059411) 7
..Oliguria (D009846)
..Polyuria (D011141) 1
..Proteinuria (D011507) 6
..Urinoma (D053584)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9120
Name:	Polyuria
Definition:	Urination of a large volume of urine with an increase in urinary frequency, commonly seen in diabetes (DIABETES MELLITUS; DIABETES INSIPIDUS).
Alternative IDs:
ParentIDs:	MESH:D014555\|MESH:D020924
TreeNumbers:	C12.777.934.616 \|C13.351.968.934.616 \|C23.888.942.600
Synonyms:	Polyurias
Slim Mappings:	Signs and symptoms\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D011141 MeSH: D011141 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants