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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: Pathologic Processes (D010335)
Parent Node: Respiration Disorders (D012120)
..Starting node ..Respiratory Aspiration (D053120)
Child Nodes:
........Respiratory Aspiration of Gastric Contents (D063466)
Sister Nodes:
..Acute Chest Syndrome (D056586)
..Altitude Sickness (D000532) 1
..Apnea (D001049) 7
..Cheyne-Stokes Respiration (D002639)
..Cough (D003371) 1
..Dyspnea (D004417) 1
..Hoarseness (D006685) 2
..Hyperventilation (D006985) 2
..Hypoglossia With Situs Inversus (C567567)
..Hypoglossia, Isolated (C567568)
..Meconium Aspiration Syndrome (D008471)
..Methionine Malabsorption Syndrome (C562682)
..Mouth Breathing (D009058)
..Respiratory Aspiration (D053120) 1
..Respiratory Distress Syndrome, Adult (D012128)
..Respiratory Distress Syndrome, Newborn (D012127) 9
..Respiratory Insufficiency (D012131) 19
..Sarcoglycanopathies (D058088) 3
..Tachypnea (D059246) 1
..Vocal Cord Dysfunction (D064706) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9681
Name:	Respiratory Aspiration
Definition:	Inhaling liquid or solids, such as stomach contents, into the RESPIRATORY TRACT. When this causes severe lung damage, it is called ASPIRATION PNEUMONIA.
Alternative IDs:
ParentIDs:	MESH:D010335\|MESH:D012120
TreeNumbers:	C08.618.749 \|C23.550.773
Synonyms:	Aspiration, Respiratory
Slim Mappings:	Pathology (process)\|Respiratory tract disease
Reference:	MedGen: D053120 MeSH: D053120 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants