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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: Pathological Conditions, Anatomical (D020763)
..Starting node ..Ventricular Remodeling (D020257)
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:	11570
Name:	Ventricular Remodeling
Definition:	The geometric and structural changes that the HEART VENTRICLES undergo, usually following MYOCARDIAL INFARCTION. It comprises expansion of the infarct and dilatation of the healthy ventricle segments. While most prevalent in the left ventricle, it can also occur in the right ventricle.
Alternative IDs:
ParentIDs:	MESH:D020763
TreeNumbers:	C23.300.985
Synonyms:	Cardiac Remodelings, Ventricular \|Cardiac Remodeling, Ventricular \|Left Ventricle Remodeling \|Left Ventricle Remodelings \|Left Ventricular Remodeling \|Left Ventricular Remodelings \|Myocardial Remodelings, Ventricular \|Myocardial Remodeling, Ventricular \|Remodeli
Slim Mappings:	Pathology (anatomical condition)
Reference:	MedGen: D020257 MeSH: D020257 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants