Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Anemia, Sickle Cell (D000755)
Parent Node: Lung Diseases (D008171)
Parent Node: Respiration Disorders (D012120)
..Starting node ..Acute Chest Syndrome (D056586)
Child Nodes:
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:	232
Name:	Acute Chest Syndrome
Definition:	Respiratory syndrome characterized by the appearance of a new pulmonary infiltrate on chest x-ray, accompanied by symptoms of fever, cough, chest pain, tachypnea, or DYSPNEA, often seen in patients with SICKLE CELL ANEMIA. Multiple factors (e.g., infection, and pulmonary FAT EMBOLISM) may contribute to the development of the syndrome.
Alternative IDs:
ParentIDs:	MESH:D000755\|MESH:D008171\|MESH:D012120
TreeNumbers:	C08.381.074 \|C08.618.009 \|C15.378.071.141.150.150.219 \|C15.378.420.155.219 \|C16.320.070.150.219 \|C16.320.365.155.219
Synonyms:	Acute Chest Syndromes \|Syndrome, Acute Chest \|Syndromes, Acute Chest
Slim Mappings:	Blood disease\|Genetic disease (inborn)\|Respiratory tract disease
Reference:	MedGen: D056586 MeSH: D056586 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants