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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

Disease Browser
Parent Node: Bronchial Diseases (D001982)
Parent Node: Cartilage Diseases (D002357)
Parent Node: Musculoskeletal Abnormalities (D009139)
Parent Node: Tracheal Diseases (D014133)
..Starting node ..Tracheobronchomalacia (D055089)
Child Nodes:
........Bronchomalacia (D055091)
........Tracheomalacia (D055090) 2
Sister Nodes:
..Novak syndrome (C537851)
..Tracheal Neoplasms (D014134)
..Tracheal Stenosis (D014135) 3
..Tracheitis (D014136)
..Tracheobronchomalacia (D055089) 4
..Tracheobronchomegaly (D014137)
..Tracheobronchopathia osteoplastica (C536977)
..Tracheoesophageal Fistula (D014138) 4
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11188
Name:	Tracheobronchomalacia
Definition:	A congenital or acquired condition of underdeveloped or degeneration of CARTILAGE in the TRACHEA and the BRONCHI. This results in a floppy non-rigid airway making patency difficult to maintain.
Alternative IDs:
ParentIDs:	MESH:D001982\|MESH:D002357\|MESH:D009139\|MESH:D014133
TreeNumbers:	C05.182.895 \|C08.127.719 \|C08.907.796 \|C16.131.621.953 \|C17.300.182.895
Synonyms:	Chondromalacia of Trachea and Bronchi \|Syndrome, Williams-Campbell \|Tracheobronchomalacias \|Williams Campbell Syndrome \|Williams-Campbell Syndrome
Slim Mappings:	Congenital abnormality\|Connective tissue disease\|Musculoskeletal disease\|Respiratory tract disease
Reference:	MedGen: D055089 MeSH: D055089 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants