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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: Ellis-Van Creveld Syndrome (D004613)
Parent Node: Situs Inversus (D012857)
..Starting node ..Jeune syndrome situs inversus (C537572)
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:	5966
Name:	Jeune syndrome situs inversus
Definition:
Alternative IDs:
ParentIDs:	MESH:D004613\|MESH:D012857
TreeNumbers:	C05.116.099.708.327/C537572 \|C16.131.077.350.398/C537572 \|C16.131.810/C537572 \|C16.131.831.350.398/C537572 \|C16.320.850.250.398/C537572 \|C17.800.804.350.398/C537572 \|C17.800.827.250.398/C537572
Synonyms:
Slim Mappings:	Congenital abnormality\|Genetic disease (inborn)\|Musculoskeletal disease\|Skin disease
Reference:	MedGen: C537572 MeSH: C537572 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants