Disease browser and phenotype portal

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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: Spinal Cord Vascular Diseases (D020758)
..Starting node ..Spinal Cord Ischemia (D020760)
Child Nodes:
........Anterior spinal artery stroke (C537776)
........Anterior Spinal Artery Syndrome (D020759)
Sister Nodes:
..Anterior Spinal Artery Syndrome (D020759)
..Spinal Cord Ischemia (D020760) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10460
Name:	Spinal Cord Ischemia
Definition:	Reduced blood flow to the spinal cord which is supplied by the anterior spinal artery and the paired posterior spinal arteries. This condition may be associated with ARTERIOSCLEROSIS, trauma, emboli, diseases of the aorta, and other disorders. Prolonged ischemia may lead to INFARCTION of spinal cord tissue.
Alternative IDs:
ParentIDs:	MESH:D020758
TreeNumbers:	C10.228.854.785.650 \|C14.907.790.550
Synonyms:	Cord Ischemia, Spinal \|Cord Ischemias, Spinal \|Experimental Spinal Cord Ischemia \|Ischemia, Spinal Cord \|Ischemias, Spinal Cord \|Ischemic Myelopathies \|Ischemic Myelopathy \|Myelopathies, Ischemic \|Myelopathy, Ischemic \|Spinal Cord Ischemia, Experimental \|Spinal Co
Slim Mappings:	Cardiovascular disease\|Nervous system disease
Reference:	MedGen: D020760 MeSH: D020760 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants