twin-to-twin transfusion syndrome |
Disease ID | 1797 |
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Disease | twin-to-twin transfusion syndrome |
Definition | Passage of blood from one fetus to another via an arteriovenous communication or other shunt, in a monozygotic twin pregnancy. It results in anemia in one twin and polycythemia in the other. (Lee et al., Wintrobe's Clinical Hematology, 9th ed, p737-8) |
Synonym | cross transfusion, intrauterine cross-transfusion, intrauterine cross-transfusions, intrauterine fetal blood loss from fetal hemorrhage into co-twin fetal transfusion syndrome fetal transfusion syndromes fetal twin to twin transfusion fetofetal transfusion fetofetal transfusion [disease/finding] fetofetal transfusion syndrome fetofetal transfusion syndromes fetofetal transfusions fetus-to-fetus placental transfusion syndrome ffts - fetofetal transfusion syndrome intrauterine cross transfusion intrauterine cross-transfusion intrauterine cross-transfusions placental transfusion syndrome stuck twin syndrome syndrome transfusion twin twin syndrome transfusion twin-twin syndrome, fetal transfusion syndrome, fetofetal transfusion syndrome, twin transfusion syndrome, twin-to-twin transfusion syndromes, fetal transfusion syndromes, fetofetal transfusion syndromes, twin transfusion syndromes, twin-to-twin transfusion transfusion syndrome, fetal transfusion syndrome, fetofetal transfusion syndrome, twin transfusion syndrome, twin-to-twin transfusion syndromes, fetal transfusion syndromes, fetofetal transfusion syndromes, twin transfusion syndromes, twin-to-twin transfusion, fetofetal transfusion, twin transfusions, fetofetal transfusions, twin ttts ttts - twin to twin transfusion syndrome twin to twin transfusion twin to twin transfusion (disorder) twin to twin transfusion syndrome twin transfusion twin transfusion syndrome twin transfusion syndromes twin transfusions twin twin transfusion twin twin transfusion syndrome twin-to-twin blood transfer twin-to-twin blood transfer (disorder) twin-to-twin transfusion syndromes twin-twin transfusion syndrome |
Orphanet | |
DOID | |
UMLS | C2909036 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:2) |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:51) 8086 | AAAS | DISEASES 56942 | CMC2 | DISEASES 2597 | GAPDH | DISEASES 7291 | TWIST1 | DISEASES 59272 | ACE2 | DISEASES 347733 | TUBB2B | DISEASES 6496 | SIX3 | DISEASES 84680 | ACCS | DISEASES 6717 | SRI | DISEASES 2252 | FGF7 | DISEASES 5972 | REN | DISEASES 7424 | VEGFC | DISEASES 2321 | FLT1 | DISEASES 4838 | NODAL | DISEASES 9317 | PTER | DISEASES 7846 | TUBA1A | DISEASES 8862 | APLN | DISEASES 27165 | GLS2 | DISEASES 8557 | TCAP | DISEASES 285 | ANGPT2 | DISEASES 151516 | ASPRV1 | DISEASES 1442 | CSH1 | DISEASES 113457 | TUBA3D | DISEASES 5069 | PAPPA | DISEASES 5671 | PSG3 | DISEASES 554 | AVPR2 | DISEASES 120 | ADD3 | DISEASES 871 | SERPINH1 | DISEASES 183 | AGT | DISEASES 7139 | TNNT2 | DISEASES 8038 | ADAM12 | DISEASES 5406 | PNLIP | DISEASES 1081 | CGA | DISEASES 26036 | ZNF451 | DISEASES 7075 | TIE1 | DISEASES 27286 | SRPX2 | DISEASES 2022 | ENG | DISEASES 5320 | PLA2G2A | DISEASES 8544 | PIR | DISEASES 6557 | SLC12A1 | DISEASES 6710 | SPTB | DISEASES 1443 | CSH2 | DISEASES 5670 | PSG2 | DISEASES 3481 | IGF2 | DISEASES 139728 | PNCK | DISEASES 30816 | ERVW-1 | DISEASES 405754 | ERVFRD-1 | DISEASES 26064 | RAI14 | DISEASES 284 | ANGPT1 | DISEASES 5228 | PGF | DISEASES 10381 | TUBB3 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1797 |
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Disease | twin-to-twin transfusion syndrome |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:3) HP:0000776 | Diaphragmatic hernia | 1 HP:0001250 | Seizures | 1 HP:0001518 | Small for gestational age | 1 |
Disease ID | 1797 |
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Disease | twin-to-twin transfusion 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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