Disease browser and phenotype portal

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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: Hemorrhage (D006470)
Parent Node: Lung Diseases (D008171)
Parent Node: Signs and Symptoms, Respiratory (D012818)
..Starting node ..Hemoptysis (D006469)
Child Nodes:
Sister Nodes:
..Anoxia (D000860) 1
..Apnea (D001049) 7
..Cheyne-Stokes Respiration (D002639)
..Cough (D003371) 1
..Dyspnea (D004417) 1
..Hemoptysis (D006469)
..Hoarseness (D006685) 2
..Hypercapnia (D006935)
..Hyperoxia (D018496)
..Hyperventilation (D006985) 2
..Hypocapnia (D016857)
..Hypoventilation (D007040) 3
..Infantile Apparent Life-Threatening Event (D057768)
..Mouth Breathing (D009058)
..Respiratory Sounds (D012135) 2
..Sneezing (D012912) 2
..Tachypnea (D059246) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5048
Name:	Hemoptysis
Definition:	Expectoration or spitting of blood originating from any part of the RESPIRATORY TRACT, usually from hemorrhage in the lung parenchyma (PULMONARY ALVEOLI) and the BRONCHIAL ARTERIES.
Alternative IDs:
ParentIDs:	MESH:D006470\|MESH:D008171\|MESH:D012818
TreeNumbers:	C08.381.348 \|C23.550.414.896 \|C23.888.852.430
Synonyms:	Hemoptyses
Slim Mappings:	Pathology (process)\|Respiratory tract disease\|Signs and symptoms
Reference:	MedGen: D006469 MeSH: D006469 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants