PedAM

Pediatric Disease Annotations & Medicines


	eisenmenger syndrome

Disease ID	1698
Disease	eisenmenger syndrome
Definition	A condition associated with VENTRICULAR SEPTAL DEFECT and other congenital heart defects that allow the mixing of pulmonary and systemic circulation, increase blood flow into the lung, and subsequent responses to low oxygen in blood. This complex is characterized by progressive PULMONARY HYPERTENSION; HYPERTROPHY of the RIGHT VENTRICLE; CYANOSIS; and ERYTHROCYTOSIS.
Synonym	complex, eisenmenger complex, eisenmenger's eisenmenger complex eisenmenger complex [disease/finding] eisenmenger defect eisenmenger's complex eisenmenger's complex (disorder) eisenmenger's defect eisenmenger's defect (disorder) eisenmenger's defect or complex eisenmenger's syndrome eisenmenger's syndrome (disorder) eisenmengers complex eisenmengers syndrome syndrome, eisenmenger syndrome, eisenmenger's
Orphanet	ORPHANET:97214
UMLS	C0013743
MeSH	D004541
SNOMED-CT	SNOMEDCT_US_2016_09_01:204311009;SNOMEDCT_US_2016_09_01:83130006;SNOMEDCT_US_2016_09_01:445928005
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:13) C0020538 \| hypertension \| 7 C0018818 \| ventricular septal defect \| 5 C1619734 \| pulmonary arterial hypertension \| 3 C0020542 \| pulmonary hypertension \| 2 C0152021 \| congenital heart disease \| 2 C0018799 \| heart disease \| 2 C0018801 \| heart failure \| 1 C0002766 \| analgesia \| 1 C0030421 \| paraganglioma \| 1 C0040053 \| thrombosis \| 1 C0026269 \| mitral stenosis \| 1 C0039730 \| thalassemia \| 1 C0018799 \| heart diseases \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	(Waiting for update.)
Locus	(Waiting for update.)

Disease ID	1698
Disease	eisenmenger syndrome
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:19) HP:0000822 \| Hypertension \| 7 HP:0001629 \| Ventricular septal defects \| 5 HP:0001631 \| Atria septal defect \| 5 HP:0001643 \| Persistent ductus arteriosus \| 4 HP:0002092 \| Pulmonary artery hypertension \| 2 HP:0003073 \| Hypoalbuminaemia \| 1 HP:0001685 \| Myocardial fibrosis \| 1 HP:0002668 \| Paragangliomas \| 1 HP:0001693 \| Cardiac shunt \| 1 HP:0002584 \| Intestinal hemorrhage \| 1 HP:0002239 \| Gastrointestinal hemorrhage \| 1 HP:0000421 \| Bloody nose \| 1 HP:0001635 \| Congestive heart failure \| 1 HP:0001714 \| Ventricular hypertrophy \| 1 HP:0004937 \| Pulmonary artery aneurysm \| 1 HP:0001718 \| Mitral stenosis \| 1 HP:0000961 \| Cyanosis \| 1 HP:0002094 \| Dyspnea \| 1 HP:0011611 \| Interrupted aortic arch \| 1

Disease ID	1698
Disease	eisenmenger syndrome
Manually Symptom	(Waiting for update.)
Text Mined Symptom	(Waiting for update.)

Manually Genotype(Total Text Mining Genotypes:0)
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All Snps(Total Genotypes:0)
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GWASdb Annotation(Total Genotypes:0)
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GWASdb Snp Trait(Total Genotypes:0)
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Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
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Chemical(Total Drugs:0)
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FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
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