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: adenocarcinoma (MONDO:0004970)
Parent Node: non-small cell lung carcinoma (disease) (MONDO:0005233)
..Starting node ..lung adenocarcinoma ()
Child Nodes:
........acinar lung adenocarcinoma ()
........Logopenic progressive aphasia ()
........lung adenocarcinoma in situ ()
........lung adenoid cystic carcinoma ()
........lung colloid adenocarcinoma ()
........lung combined type small cell adenocarcinoma ()
........lung occult adenocarcinoma ()
........lung signet ring cell carcinoma ()
........minimally invasive lung adenocarcinoma ()
........papillary lung adenocarcinoma ()
........well-differentiated fetal adenocarcinoma of the lung ()
Sister Nodes:
..lung adenocarcinoma ()
..lung large cell carcinoma ()
..non-small cell squamous lung carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5061
Name:	lung adenocarcinoma
Definition:	A carcinoma that arises from the lung and is characterized by the presence of malignant glandular epithelial cells. There is a male predilection with a male to female ratio of 2:1. Usually lung adenocarcinoma is asymptomatic and is identified through screening studies or as an incidental radiologic finding. If clinical symptoms are present they include shortness of breath, cough, hemoptysis, chest pain, and fever. Tobacco smoke is a known risk factor.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of lung; adenocarcinoma of the lung; bronchogenic lung adenocarcinoma; lung adenocarcinoma; non-small cell lung adenocarcinoma; nonsmall cell adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal