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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 Diseases (D013118)
Parent Node: Spinal Cord Injuries (D013119)
..Starting node ..Spinal Cord Compression (D013117)
Child Nodes:
Sister Nodes:
..Autonomic Dysreflexia (D020211)
..Central Cord Syndrome (D020210)
..Spinal Cord Compression (D013117)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10457
Name:	Spinal Cord Compression
Definition:	Acute and chronic conditions characterized by external mechanical compression of the SPINAL CORD due to extramedullary neoplasm; EPIDURAL ABSCESS; SPINAL FRACTURES; bony deformities of the vertebral bodies; and other conditions. Clinical manifestations vary with the anatomic site of the lesion and may include localized pain, weakness, sensory loss, incontinence, and impotence.
Alternative IDs:
ParentIDs:	MESH:D013118\|MESH:D013119
TreeNumbers:	C10.228.854.761 \|C26.819.678
Synonyms:	Compression, Spinal Cord \|Compressions, Spinal Cord \|Compressive Myelopathy \|Conus Medullaris Syndrome \|Conus Medullaris Syndromes \|Extramedullary Spinal Cord Compression \|Myelopathy, Compressive \|Spinal Cord Compression, Extramedullary \|Spinal Cord Compressions
Slim Mappings:	Nervous system disease\|Wounds and injuries
Reference:	MedGen: D013117 MeSH: D013117 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants