MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation 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

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

Disease Browser
Parent Node: benign neoplasm (MONDO:0005165)
Parent Node: neoplasm of thorax (MONDO:0021350)
..Starting node ..thoracic benign neoplasm ()
Child 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 ()
Sister Nodes:
..axillary neoplasm ()
..breast neoplasm ()
..bronchial neoplasm (disease) ()
..heart neoplasm ()
..lung neoplasm ()
..neoplasm of chest wall ()
..neoplasm of esophagus ()
..neoplasm of mediastinum ()
..neoplasm of pericardium ()
..sternal neoplasm ()
..thoracic benign neoplasm ()
..thoracic cancer ()
..thymus neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	634
Name:	thoracic benign neoplasm
Definition:	A non-metastasizing neoplasm arising from any of the organs of the thoracic cavity. Representative examples include pleural adenomatoid tumor, chest wall lipoma, mediastinal schwannoma, and lung hamartoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign neoplasm of the thorax; benign neoplasm of thorax; benign thoracic neoplasm; benign thoracic tumor; benign tumor of the thorax; benign tumor of thorax; thoracic segment of trunk benign neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: SLC11A2;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal