Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Oral Fistula (D016155)
Parent Node: Salivary Gland Diseases (D012466)
..Starting node ..Salivary Gland Fistula (D012467)
Child Nodes:
Sister Nodes:
..Aplasia of Lacrimal and Salivary Glands (C562407)
..Mikulicz' Disease (D008882)
..Parotid Diseases (D010305) 7
..Parotid Salivary Glands, Polycystic Disease of (C563951)
..Salivary Calculi (D020792) 2
..Salivary Gland Fistula (D012467)
..Salivary Gland Neoplasms (D012468) 6
..Sialadenitis (D012793) 6
..Sialometaplasia, Necrotizing (D012797)
..Sialorrhea (D012798)
..Submandibular Gland Diseases (D013364) 1
..Tunglang Savage Bellman syndrome (C536927)
..Xerostomia (D014987) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9953
Name:	Salivary Gland Fistula
Definition:	A fistula between a salivary duct or gland and the cutaneous surface of the oral cavity.
Alternative IDs:
ParentIDs:	MESH:D012466\|MESH:D016155
TreeNumbers:	C07.465.614.655 \|C07.465.815.655 \|C23.300.575.500.775
Synonyms:	Fistula, Salivary Gland \|Fistulas, Salivary Gland \|Gland Fistula, Salivary \|Gland Fistulas, Salivary \|Salivary Gland Fistulas
Slim Mappings:	Mouth disease\|Pathology (anatomical condition)
Reference:	MedGen: D012467 MeSH: D012467 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants