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 mediastinum (MONDO:0021386)
Parent Node: thoracic benign neoplasm (MONDO:0000634)
..Starting node ..benign neoplasm of mediastinum ()
Child Nodes:
........mediastinal schwannoma ()
........mediastinum leiomyoma ()
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:	21521
Name:	benign neoplasm of mediastinum
Definition:	A benign neoplasm that involves the mediastinum.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign mediastinal neoplasm; benign mediastinal neoplasms NOS; benign mediastinal tumor; benign neoplasm of the mediastinum; benign tumor of mediastinum; benign tumor of the mediastinum; mediastinum benign neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal