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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: Heart Defects, Congenital (D006330)
Parent Node: Situs Inversus (D012857)
..Starting node ..Dextrocardia (D003914)
Child Nodes:
........Aughton syndrome (C538269)
........Heterotaxy, visceral, X-linked (C538116)
........Kartagener Syndrome (D007619) 6
........Kennerknecht Sorgo Oberhoffer syndrome (C537018)
Sister Nodes:
..Dextrocardia (D003914) 10
..Fraser Jequier Chen syndrome (C535481)
..HETEROTAXY, VISCERAL, 5, AUTOSOMAL (OMIM:270100)
..Hypoglossia With Situs Inversus (C567567)
..Jeune syndrome situs inversus (C537572)
..Levocardia (D007979)
..Marfanoid Habitus with Situs Inversus (C563814)
..RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
..Situs inversus totalis with cystic dysplasia of kidneys and pancreas (C536666)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3261
Name:	Dextrocardia
Definition:	A congenital defect in which the heart is located on the right side of the THORAX instead of on the left side (levocardia, the normal position). When dextrocardia is accompanied with inverted HEART ATRIA, a right-sided STOMACH, and a left-sided LIVER, the combination is called dextrocardia with SITUS INVERSUS. Dextrocardia may adversely affect other thoracic organs.
Alternative IDs:
ParentIDs:	MESH:D006330\|MESH:D012857
TreeNumbers:	C14.240.400.280 \|C14.280.400.280 \|C16.131.240.400.280 \|C16.131.810.250
Synonyms:	Dextrocardias
Slim Mappings:	Cardiovascular disease\|Congenital abnormality
Reference:	MedGen: D003914 MeSH: D003914 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants