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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: Lung Diseases (D008171)
Parent Node: Respiratory System Abnormalities (D015619)
..Starting node ..Cystic Adenomatoid Malformation of Lung, Congenital (D015615)
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:	2932
Name:	Cystic Adenomatoid Malformation of Lung, Congenital
Definition:	An abnormality in lung development that is characterized by a multicystic mass resulting from an adenomatous overgrowth of the terminal BRONCHIOLES with a consequent reduction of PULMONARY ALVEOLI. This anomaly is classified into three types by the cyst size.
Alternative IDs:
ParentIDs:	MESH:D008171\|MESH:D015619
TreeNumbers:	C08.381.150 \|C08.695.290 \|C16.131.740.290
Synonyms:	Congenital Cystic Adenomatoid Malformation \|Congenital Cystic Adenomatoid Malformation of Lung \|Congenital Cystic Adenomatoid Malformation, Type 1 \|Congenital Cystic Adenomatoid Malformation, Type 2 \|Congenital Cystic Adenomatoid Malformation, Type 3 \|Congeni
Slim Mappings:	Congenital abnormality\|Respiratory tract disease
Reference:	MedGen: D015615 MeSH: D015615 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants