Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Arterial Occlusive Diseases (D001157)
..Starting node ..Fibromuscular Dysplasia (D005352)
Child Nodes:
........Fibromuscular dysplasia of arteries (C537929)
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:	4287
Name:	Fibromuscular Dysplasia
Definition:	An idiopathic, segmental, nonatheromatous disease of the musculature of arterial walls, leading to STENOSIS of small and medium-sized arteries. There is true proliferation of SMOOTH MUSCLE CELLS and fibrous tissue. Fibromuscular dysplasia lesions are smooth stenosis and occur most often in the renal and carotid arteries. They may also occur in other peripheral arteries of the extremity.
Alternative IDs:
ParentIDs:	MESH:D001157
TreeNumbers:	C14.907.137.372
Synonyms:	Dysplasia, Fibromuscular \|Dysplasias, Fibromuscular \|Fibromuscular Dysplasias
Slim Mappings:	Cardiovascular disease
Reference:	MedGen: D005352 MeSH: D005352 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants