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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: Osteochondrodysplasias (D010009)
Parent Node: Tracheal Diseases (D014133)
..Starting node ..Tracheobronchopathia osteoplastica (C536977)
Child Nodes:
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:	11190
Name:	Tracheobronchopathia osteoplastica
Definition:
Alternative IDs:
ParentIDs:	MESH:D010009\|MESH:D014133
TreeNumbers:	C05.116.099.708/C536977 \|C08.907/C536977
Synonyms:	Cartilaginous or bony projections into the tracheobronchial lumen \|Tracheobronchopathia Osteochondroplastica \|Tracheopathia osteoplastica
Slim Mappings:	Musculoskeletal disease\|Respiratory tract disease
Reference:	MedGen: C536977 MeSH: C536977 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants