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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: Cysts (D003560)
Parent Node: Respiratory System Abnormalities (D015619)
..Starting node ..Bronchogenic Cyst (D001994)
Child Nodes:
Sister Nodes:
..Bronchogenic Cyst (D001994)
..Bronchopulmonary Sequestration (D001998)
..Choanal Atresia (D002754) 8
..Cystic Adenomatoid Malformation of Lung, Congenital (D015615)
..Fraser-Like Syndrome (C565562)
..Kartagener Syndrome (D007619) 6
..Laryngocele (D059608)
..Laryngostenosis (D007829)
..Oculoauriculofrontonasal syndrome (C537865)
..Scimitar Syndrome (D012587) 1
..Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs (C567517)
..Tracheobronchomegaly (D014137)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1502
Name:	Bronchogenic Cyst
Definition:	A usually spherical cyst, arising as an embryonic out-pouching of the foregut or trachea. It is generally found in the mediastinum or lung and is usually asymptomatic unless it becomes infected.
Alternative IDs:
ParentIDs:	MESH:D001982\|MESH:D003560\|MESH:D015619
TreeNumbers:	C04.182.195 \|C08.127.480 \|C08.695.195 \|C16.131.740.195
Synonyms:	Bronchial Cyst \|Bronchial Cysts \|Bronchogenic Cysts \|Cyst, Bronchial \|Cyst, Bronchogenic \|Cysts, Bronchial \|Cysts, Bronchogenic
Slim Mappings:	Cancer\|Congenital abnormality\|Respiratory tract disease
Reference:	MedGen: D001994 MeSH: D001994 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants