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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: Pathologic Processes (D010335)
Parent Node: Pathological Conditions, Anatomical (D020763)
..Starting node ..Vascular Remodeling (D066253)
Child Nodes:
Sister Nodes:
..Accessory Atrioventricular Bundle (D058606)
..Agenesis of Corpus Callosum (D061085) 59
..Airway Remodeling (D056151)
..Alopecia (D000505) 61
..Atrial Remodeling (D064752)
..Atrophy (D001284) 18
..Blister (D001768) 3
..Calculi (D002137) 15
..Choristoma (D002828) 2
..Constriction, Pathologic (D003251) 9
..Cysts (D003560) 78
..Dilatation, Pathologic (D004108)
..Diverticulum (D004240) 7
..Facial Asymmetry (D005146) 8
..Fistula (D005402) 34
..Hernia (D006547) 73
..Hypertrophy (D006984) 62
..Leg Length Inequality (D007870)
..Leukoplakia (D007971) 2
..Nails, Malformed (D009264) 44
..Plaque, Amyloid (D058225) 1
..Plaque, Atherosclerotic (D058226)
..Polyps (D011127) 7
..Prolapse (D011391) 5
..Rupture, Spontaneous (D012422) 1
..Torsion Abnormality (D014102) 13
..Vascular Remodeling (D066253)
..Ventricular Remodeling (D020257)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11535
Name:	Vascular Remodeling
Definition:	The active alterations of vascular wall structures, often leading to elevated VASCULAR RESISTANCE. It is associated with AGING; ATHEROSCLEROSIS; DIABETES MELLITUS; HYPERTENSION; PREGNANCY; PULMONARY HYPERTENSION; and STROKE, but is also a normal part of EMBRYOGENESIS.
Alternative IDs:
ParentIDs:	MESH:D010335\|MESH:D020763
TreeNumbers:	C23.300.977 \|C23.550.918
Synonyms:	Arterial Remodeling, Pulmonary \|Arterial Remodelings, Pulmonary \|Pulmonary Arterial Remodeling \|Pulmonary Arterial Remodelings \|Remodeling, Pulmonary Arterial \|Remodelings, Pulmonary Arterial \|Remodelings, Vascular \|Remodeling, Vascular \|Vascular Remodelings
Slim Mappings:	Pathology (anatomical condition)\|Pathology (process)
Reference:	MedGen: D066253 MeSH: D066253 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants