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: neoplasm of chest wall (MONDO:0021388)
Parent Node: thoracic benign neoplasm (MONDO:0000634)
..Starting node ..benign neoplasm of chest wall ()
Child Nodes:
........chest wall lipoma ()
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:	21529
Name:	benign neoplasm of chest wall
Definition:	A benign neoplasm that involves the chest wall.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign chest wall neoplasm; benign chest wall tumor; benign neoplasm of the chest wall; benign tumor of chest wall; benign tumor of the chest wall; chest wall benign neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal