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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: Water-Electrolyte Imbalance (D014883)
..Starting node ..Dehydration (D003681)
Child Nodes:
Sister Nodes:
..Dehydration (D003681)
..Hypercalcemia (D006934) 10
..Hyperkalemia (D006947) 4
..Hypernatremia (D006955)
..Hypocalcemia (D006996) 5
..Hypokalemia (D007008) 1
..Hyponatremia (D007010) 1
..Inappropriate ADH Syndrome (D007177) 1
..Water Intoxication (D014869)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3150
Name:	Dehydration
Definition:	The condition that results from excessive loss of water from a living organism.
Alternative IDs:
ParentIDs:	MESH:D010335\|MESH:D014883
TreeNumbers:	C18.452.950.179 \|C23.550.274
Synonyms:	Stress, Water \|Water Stress
Slim Mappings:	Metabolic disease\|Pathology (process)
Reference:	MedGen: D003681 MeSH: D003681 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants