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: lung neoplasm (MONDO:0021117)
Parent Node: respiratory system benign neoplasm (MONDO:0000382)
Parent Node: thoracic benign neoplasm (MONDO:0000634)
..Starting node ..lung benign neoplasm ()
Child Nodes:
........clear cell-sugar-tumor of the lung ()
........hemangioma of lung ()
........lung adenoma ()
........lung leiomyoma ()
........lung 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:	2732
Name:	lung benign neoplasm
Definition:	A non-metastasizing neoplasm that arises from the lung parenchyma or the bronchi. Representative examples include lung adenoma, lung hamartoma, and endobronchial lipoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign lung neoplasm; benign lung tumor; benign neoplasm of lung; benign neoplasm of the lung; benign tumor of lung; benign tumor of the lung; lung benign neoplasm; tumor of the lung
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal