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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: Parasitic Diseases (D010272)
Parent Node: Respiratory Tract Infections (D012141)
..Starting node ..Lung Diseases, Parasitic (D008174)
Child Nodes:
........Echinococcosis, Pulmonary (D004445)
Sister Nodes:
..Bovine Respiratory Disease Complex (D048090) 3
..Bronchitis (D001991) 7
..Common Cold (D003139)
..Empyema, Pleural (D016724) 1
..Influenza, Human (D007251)
..Inhalation anthrax (C571912)
..Laryngitis (D007827) 1
..Legionellosis (D007876) 1
..Lung Abscess (D008169)
..Lung Diseases, Fungal (D008172) 5
..Lung Diseases, Parasitic (D008174) 1
..Pharyngitis (D010612) 4
..Pleurisy (D010998) 1
..Pneumonia (D011014) 16
..Recurrent respiratory papillomatosis (C535297)
..Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness (C567595)
..Rhinitis (D012220) 6
..Rhinoscleroma (D012226)
..Severe Acute Respiratory Syndrome (D045169)
..Sinusitis (D012852) 5
..Supraglottitis (D059525) 1
..Tracheitis (D014136)
..Tuberculosis, Laryngeal (D014387)
..Tuberculosis, Pleural (D014396) 1
..Tuberculosis, Pulmonary (D014397) 1
..Whooping Cough (D014917)
..Young Syndrome (C536718)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6565
Name:	Lung Diseases, Parasitic
Definition:	Infections of the lungs with parasites, most commonly by parasitic worms (HELMINTHS).
Alternative IDs:
ParentIDs:	MESH:D008171\|MESH:D010272\|MESH:D012141
TreeNumbers:	C03.582 \|C08.381.517 \|C08.730.450
Synonyms:	Lung Disease, Parasitic \|Lung Parasitic Infection \|Lung Parasitic Infections \|Parasitic Infection, Pulmonary \|Parasitic Infections of Lung \|Parasitic Infections, Pulmonary \|Parasitic Lung Disease \|Parasitic Lung Diseases \|Pulmonary Parasitic Infection \|Pulmonary
Slim Mappings:	Parasitic disease\|Respiratory tract disease
Reference:	MedGen: D008174 MeSH: D008174 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants