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: bronchial disease (MONDO:0001358)
Parent Node: neoplasm of thorax (MONDO:0021350)
Parent Node: respiratory tract neoplasm (MONDO:0020641)
..Starting node ..bronchial neoplasm (disease) ()
Child Nodes:
........bronchial endocrine tumor ()
........bronchus adenoma ()
........bronchus cancer ()
........endobronchial leiomyoma ()
........endobronchial lipoma ()
Sister Nodes:
..bronchial neoplasm (disease) ()
..laryngeal neoplasm ()
..lung neoplasm ()
..nasal cavity neoplasm ()
..nasopharyngeal neoplasm ()
..pleural neoplasm ()
..rare bronchopulmonary tumor ()
..SMARCA4-deficient sarcoma of thorax ()
..trachea neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2807
Name:	bronchial neoplasm (disease)
Definition:	Tumors or cancer of the bronchi.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	bronchial neoplasm; bronchus neoplasm; bronchus neoplasm (disease); bronchus tumor; neoplasm of bronchus; tumor of bronchus
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal