MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation 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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: benign digestive system neoplasm (MONDO:0000385)
Parent Node: neoplasm of esophagus (MONDO:0021355)
Parent Node: thoracic benign neoplasm (MONDO:0000634)
..Starting node ..benign neoplasm of esophagus ()
Child Nodes:
........esophageal lipoma ()
........esophagus leiomyoma ()
........esophagus squamous cell papilloma ()
Sister Nodes:
..benign axillary neoplasm ()
..benign neoplasm of chest wall ()
..benign neoplasm of esophagus ()
..benign neoplasm of heart ()
..benign neoplasm of mediastinum ()
..benign neoplasm of pericardium ()
..benign neoplasm of sternum ()
..benign neoplasm of thymus ()
..breast benign neoplasm ()
..endobronchial lipoma ()
..lung benign neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21459
Name:	benign neoplasm of esophagus
Definition:	A benign neoplasm that involves the esophagus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign esophageal neoplasm; benign esophageal tumor; benign esophagus neoplasm; benign esophagus tumor; benign neoplasm of the esophagus; benign tumor of esophagus; benign tumor of the esophagus; esophagus benign neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal