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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: Brain Ischemia (D002545)
Parent Node: Hypoxia, Brain (D002534)
..Starting node ..Hypoxia-Ischemia, Brain (D020925)
Child Nodes:
........Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency (C566449)
Sister Nodes:
..Hypoxia-Ischemia, Brain (D020925) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5662
Name:	Hypoxia-Ischemia, Brain
Definition:	A disorder characterized by a reduction of oxygen in the blood combined with reduced blood flow (ISCHEMIA) to the brain from a localized obstruction of a cerebral artery or from systemic hypoperfusion. Prolonged hypoxia-ischemia is associated with ISCHEMIC ATTACK, TRANSIENT; BRAIN INFARCTION; BRAIN EDEMA; COMA; and other conditions.
Alternative IDs:
ParentIDs:	MESH:D002534\|MESH:D002545
TreeNumbers:	C10.228.140.300.150.716 \|C10.228.140.624.500 \|C14.907.253.092.716
Synonyms:	Anoxia Ischemia, Brain \|Anoxia-Ischemia, Brain \|Anoxia Ischemia, Cerebral \|Anoxia-Ischemia, Cerebral \|Anoxia-Ischemias, Brain \|Anoxia-Ischemias, Cerebral \|Anoxic-Ischemic Encephalopathies \|Anoxic Ischemic Encephalopathy \|Anoxic-Ischemic Encephalopathy \|Brain Anox
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D020925 MeSH: D020925 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants