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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: Pathologic Processes (D010335)
Parent Node: Uremia (D014511)
..Starting node ..Azotemia (D053099)
Child Nodes:
Sister Nodes:
..Azotemia (D053099)
..Hemolytic-Uremic Syndrome (D006463) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1117
Name:	Azotemia
Definition:	A biochemical abnormality referring to an elevation of BLOOD UREA NITROGEN and CREATININE. Azotemia can be produced by KIDNEY DISEASES or other extrarenal disorders. When azotemia becomes associated with a constellation of clinical signs, it is termed UREMIA.
Alternative IDs:
ParentIDs:	MESH:D010335\|MESH:D014511
TreeNumbers:	C12.777.419.936.231 \|C13.351.968.419.936.231 \|C23.550.145
Synonyms:
Slim Mappings:	Pathology (process)\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: D053099 MeSH: D053099 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants