pulmonary venous return anomaly |
Disease ID | 1144 |
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Disease | pulmonary venous return anomaly |
Definition | An anomalous pulmonary venous return in which the right PULMONARY VEIN is not connected to the LEFT ATRIUM but to the INFERIOR VENA CAVA. Scimitar syndrome is named for the crescent- or Turkish sword-like shadow in the chest radiography and is often associated with hypoplasia of the right lung and right pulmonary artery, and dextroposition of the heart. |
Synonym | anomalous pulmonary venous return anomaly, scimitar apvr pulmonary venolobar syndrome pulmonary venous return, anomalous, total scimitar anomaly scimitar syndrome scimitar syndrome (disorder) scimitar syndrome [disease/finding] syndrome, scimitar tapvc - total anomalous pulmonary venous connection tapvd tapvd - total anomalous pulmonary venous drainage tapvr tapvr1 tot anom pulm ven connec total anomalous pulmonary venous connection total anomalous pulmonary venous drainage total anomalous pulmonary venous return total anomalous pulmonary venous return (disorder) total anomalous pulmonary venous return 1 total anomalous pulmonary venous return nos total anomalous pulmonary venous return nos (disorder) |
Orphanet | |
OMIM | |
DOID | |
ICD10 | |
UMLS | C0036400 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:18) C0020542 | pulmonary hypertension | 2 C0158699 | renal agenesis | 2 C0008924 | cleft lip | 1 C0041408 | turner syndrome | 1 C0242379 | lung cancer | 1 C0175703 | tar syndrome | 1 C0040053 | thrombosis | 1 C0020538 | hypertension | 1 C0013069 | double outlet right ventricle | 1 C0026266 | mitral regurgitation | 1 C0085113 | neurofibromatosis | 1 C1619734 | pulmonary arterial hypertension | 1 C0026265 | mitral valve disease | 1 C0152101 | hypoplastic left heart syndrome | 1 C0155773 | portal vein thrombosis | 1 C0152101 | hypoplastic left heart | 1 C0003857 | arteriovenous malformation | 1 C0016522 | secundum atrial septal defect | 1 |
Curated Gene | Entrez_id | Symbol | Resource(Total Genes:2) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:23) 34 | ACADM | 4.443 | DISEASES 94 | ACVRL1 | 1.74 | DISEASES 27063 | ANKRD1 | 4.146 | DISEASES 554 | AVPR2 | 1.53 | DISEASES 100130418 | CECR7 | 4.378 | DISEASES 78987 | CRELD1 | 4.067 | DISEASES 79947 | DHDDS | 2.068 | DISEASES 10938 | EHD1 | 2.291 | DISEASES 2200 | FBN1 | 1.608 | DISEASES 9446 | GSTO1 | 2.19 | DISEASES 23493 | HEY2 | 2.57 | DISEASES 3767 | KCNJ11 | 1.985 | DISEASES 11012 | KLK11 | 2.674 | DISEASES 3949 | LDLR | 1.225 | DISEASES 4878 | NPPA | 1.56 | DISEASES 5154 | PDGFA | 1.926 | DISEASES 9124 | PDLIM1 | 2.332 | DISEASES 5698 | PSMB9 | 2.205 | DISEASES 5817 | PVR | 2.852 | DISEASES 135250 | RAET1E | 2.794 | DISEASES 6444 | SGCD | 2.441 | DISEASES 7433 | VIPR1 | 2.509 | DISEASES 8565 | YARS | 2.449 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1144 |
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Disease | pulmonary venous return anomaly |
Manually Symptom | (Waiting for update.) |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:1) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs142354133 | 18273862 | 27063 | ANKRD1 | umls:C0036400 | UNIPROT | Transcriptional deregulation and a missense mutation define ANKRD1 as a candidate gene for total anomalous pulmonary venous return. | 0.120271442 | 2008 | ANKRD1 | 10 | 90918971 | G | A |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:3) | ||||
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HP ID | HP Name | MP ID | MP Name | Annotation |
HP:0008386 | Aplasia/Hypoplasia of the nails | MP:0008530 | abnormal rostral-caudal patterning of the somites | anomaly in the developmental pattern of the somites along the axis that runs from the rostral to the caudal region of the body |
HP:0002205 | Recurrent respiratory infections | MP:0014182 | decreased respiratory epithelial sodium ion transmembrane transport | decrease in the directed movement of sodium ions from one side of the respiratory epithelial cell membrane to the other |
HP:0002092 | Pulmonary hypertension | MP:0005258 | ocular hypertension | abnormal elevation of the intraocular pressure |
Mapped by homologous gene(Total Items:5) | ||||
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HP ID | HP Name | MP ID | MP Name | Annotation |
HP:0005160 | Total anomalous pulmonary venous return | MP:0013600 | testis degeneration | a retrogressive impairment of function or destruction of either or both of the male reproductive glands |
HP:0002205 | Recurrent respiratory infections | MP:0020321 | increased vascular endothelial cell apoptosis | increase in the timing or the number of vascular endothelial cells undergoing programmed cell death |
HP:0002092 | Pulmonary hypertension | MP:0020254 | decreased collagen level | decreased level of the main structural protein of the various connective tissues in animals |
HP:0008386 | Aplasia/Hypoplasia of the nails | MP:0014198 | absent pituitary infundibular stalk | absence of the apical portion of the tubular structure extending from the hypothalamus to the posterior lobe of the pituitary gland |
HP:0009884 | Tapered distal phalanges of finger | MP:0013278 | decreased fasted circulating glucose level | reduction in the amount of glucose in the blood at some defined time point after eating compared to controls |
Disease ID | 1144 |
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Disease | pulmonary venous return anomaly |
Case | (Waiting for update.) |