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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: Aortic Diseases (D001018)
Parent Node: Arterial Occlusive Diseases (D001157)
..Starting node ..Leriche Syndrome (D007925)
Child Nodes:
Sister Nodes:
..Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly (C566529)
..Arteriosclerosis (D001161) 22
..Carotid Stenosis (D016893)
..Fibromuscular Dysplasia (D005352) 1
..Leriche Syndrome (D007925)
..Malignant Atrophic Papulosis (D054853)
..Mesenteric Vascular Occlusion (D008641)
..Moyamoya Disease (D009072) 4
..Peripheral Arterial Occlusive Disease 1 (C564658)
..Renal Artery Obstruction (D012078)
..Retinal Artery Occlusion (D015356) 1
..Thromboangiitis Obliterans (D013919)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6319
Name:	Leriche Syndrome
Definition:	A condition caused by occlusion of terminal aorta, the primary branches of the ABDOMINAL AORTA, as in aortoiliac obstruction. Leriche syndrome usually occurs in males and is characterized by IMPOTENCE, absence of a pulse in the femoral arteries, weakness and numbness in the lower back, buttocks, hips, and lower limbs.
Alternative IDs:
ParentIDs:	MESH:D001018\|MESH:D001157
TreeNumbers:	C14.907.109.661 \|C14.907.137.427
Synonyms:	Leriche's Syndrome \|Leriches Syndrome \|Syndrome, Leriche \|Syndrome, Leriche's
Slim Mappings:	Cardiovascular disease
Reference:	MedGen: D007925 MeSH: D007925 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants