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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: Digestive System Abnormalities (D004065)
..Starting node ..Absent duct of Santorini (C535567)
Child Nodes:
Sister Nodes:
..Absent duct of Santorini (C535567)
..Acrorenal mandibular syndrome (C535665)
..Acrorenal syndrome recessive (C535666)
..Anus, Imperforate (D001006) 21
..Barrett Esophagus (D001471) 1
..Biliary Atresia (D001656) 2
..Choledochal Cyst (D015529) 2
..Craniosynostosis, anal anomalies, and porokeratosis (C536789)
..Currarino triad (C536221)
..Diaphragmatic Eventration (D003965) 1
..Esophageal Atresia (D004933) 2
..Hirschsprung Disease (D006627) 22
..Intestinal Atresia (D007409) 11
..Meckel Diverticulum (D008467)
..VACTERL Association With Hydrocephalus (C564751)
..Volvulus Of Midgut (C562456)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	104
Name:	Absent duct of Santorini
Definition:
Alternative IDs:
ParentIDs:	MESH:D004065
TreeNumbers:	C06.198/C535567 \|C16.131.314/C535567
Synonyms:	Absent accessory pancreatic duct of Santorini
Slim Mappings:	Congenital abnormality\|Digestive system disease
Reference:	MedGen: C535567 MeSH: C535567 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants