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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 ..Levocardia (D007979)
Child Nodes:
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:	6412
Name:	Levocardia
Definition:	Congenital abnormalities in which the HEART is in the normal position (levocardia) in the left side of the chest but some or all of the THORAX or ABDOMEN viscera are transposed laterally (SITUS INVERSUS). It is also known as situs inversus with levocardia, or isolated levocardia. This condition is often associated with severe heart defects and splenic abnormalities such as asplenia or polysplenia.
Alternative IDs:
ParentIDs:	MESH:D006330\|MESH:D012857
TreeNumbers:	C14.240.400.701 \|C14.280.400.701 \|C16.131.240.400.701 \|C16.131.810.700
Synonyms:	Isolated Levocardia \|Levocardia, Isolated \|Situs Inversus with Levocardia
Slim Mappings:	Cardiovascular disease\|Congenital abnormality
Reference:	MedGen: D007979 MeSH: D007979 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants