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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: Constriction, Pathologic (D003251)
..Starting node ..Tracheal agenesis (C536975)
Child Nodes:
Sister Nodes:
..Calabro syndrome (C537960)
..Celiac Artery Stenosis from Compression by Median Arcuate Ligament of Diaphragm (C566151)
..Infundibulopelvic dysgenesis (C535528)
..Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy (C566379)
..Lumbar Stenosis, Familial (C563613)
..Pseudoainhum (C535821)
..Tracheal agenesis (C536975)
..Tracheobronchial Stenosis, Congenital (C566362)
..Urethral obstruction sequence (C536477)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11181
Name:	Tracheal agenesis
Definition:
Alternative IDs:
ParentIDs:	MESH:D003251
TreeNumbers:	C23.300.287/C536975
Synonyms:	Congenital tracheal agenesis \|Congenital tracheal stenosis
Slim Mappings:	Pathology (anatomical condition)
Reference:	MedGen: C536975 MeSH: C536975 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants