Disease browser and phenotype portal

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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 Fistula (D016154)
Parent Node: Pancreatic Diseases (D010182)
..Starting node ..Pancreatic Fistula (D010185)
Child Nodes:
Sister Nodes:
..Annular pancreas (C536376)
..Congenital Hyperinsulinism (D044903) 2
..Cystic Fibrosis (D003550) 4
..Exocrine Pancreatic Insufficiency (D010188) 3
..Johanson Blizzard syndrome (C535880)
..Pancreatic Agenesis, Congenital (C564908)
..Pancreatic Cyst (D010181) 2
..Pancreatic Fistula (D010185)
..Pancreatic lipomatosis duodenal stenosis (C535839)
..Pancreatic Neoplasms (D010190) 20
..Pancreatitis (D010195) 8
..RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8545
Name:	Pancreatic Fistula
Definition:	Abnormal passage communicating with the PANCREAS.
Alternative IDs:
ParentIDs:	MESH:D010182\|MESH:D016154
TreeNumbers:	C06.267.775 \|C06.689.583 \|C23.300.575.185.775
Synonyms:	Fistula, Pancreatic \|Fistulas, Pancreatic \|Pancreatic Fistulas
Slim Mappings:	Digestive system disease\|Pathology (anatomical condition)
Reference:	MedGen: D010185 MeSH: D010185 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants