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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, Signs and Symptoms (D013568)
..Starting node ..Pathological Conditions, Anatomical (D020763)
Child 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)
Sister Nodes:
..Morphological and Microscopic Findings (D065308) 3
..Pathologic Processes (D010335) 1132
..Pathological Conditions, Anatomical (D020763) 522
..Signs and Symptoms (D012816) 1837
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8720
Name:	Pathological Conditions, Anatomical
Definition:	An abnormal structural condition of the human body, usually macroscopic, that is common to a variety of different diseases.
Alternative IDs:
ParentIDs:	MESH:D013568
TreeNumbers:	C23.300
Synonyms:	Anatomical Pathological Condition \|Anatomical Pathological Conditions \|Condition, Anatomical Pathological \|Conditions, Anatomical Pathological \|Pathological Condition, Anatomical
Slim Mappings:	Pathology (anatomical condition)
Reference:	MedGen: D020763 MeSH: D020763 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants