| Rank (Similarity) |
PMID (PMCID) |
|
|---|---|---|
| 1 (37.5%) |
25806676 |
Intestinal Anastomotic Ulcers in Children With Short Bowel Syndrome and Anemia Detected by Capsule Endoscopy. Bass LM, Zimont J, Prozialeck J, Superina R, Cohran V. J Pediatr Gastroenterol Nutr. 2015;61(2):215-9. |
| Anemia Enterocolitis | ||
| Anemia Capsule Endoscopy Child Child, Preschool Females Gastrointestinal Hemorrhage Homo sapiens Intestinal Diseases Male Retrospective Studies Short Bowel Syndrome Ulcer | ||
| 2 (37.1%) |
18338135 |
Neonatal haemochromatosis associated with gastroschisis. Thornton MP, Marven SS, Tanner MS, Gurtl-Lackner B. Pediatr Surg Int. 2008;24(5):637-9. |
| Jaundice Thrombocytopenia | ||
| Differential Diagnosis Fatal Outcome Gastroschisis Hemochromatosis Homo sapiens Infant, Newborn Male | ||
| 3 (36.3%) |
10532267 |
Hepatopathy in two infants with short-bowel syndrome and cytomegalovirus infection. Ensenauer R, Hentschel R, Ruckauer K, Radecke J, Brandis M, Berner R. Eur J Pediatr Surg. 1999;9(4):244-7. |
| Cholestasis Thrombocytopenia | ||
| Cytomegalovirus Infections Fatal Outcome Females Homo sapiens Infant Infant, Newborn Liver Failure Male Parenteral Nutrition Short Bowel Syndrome | ||
| 4 (33.0%) |
23845650 |
Staple line ulcers: a cause of chronic GI bleeding following STEP procedure. Gibbons TE, Casteel HB, Vaughan JF, Dassinger MS. J Pediatr Surg. 2013;48(6):E1-3. |
| Overgrowth Anemia Vascular dilatation | ||
| Capsule Endoscopy Child Digestive System Surgical Procedures Gastrointestinal Hemorrhage Homo sapiens Intestines, Small Postoperative Complications Short Bowel Syndrome Ulcer | ||
| 5 (29.2%) |
2401946 |
The blind loop syndrome in children. Stewart BA, Karrer FM, Hall RJ, Lilly JR. J Pediatr Surg. 1990;25(8):905-8. |
| Cirrhosis Hypoalbuminemia Biliary atresia | ||
| Bacterial Infections Biliary Atresia Blind Loop Syndrome Child, Preschool Females Gastrointestinal Motility Homo sapiens Infant Infant, Newborn Male Repeat Surgery | ||
| 6 (26.6%) |
19582443 |
Delayed, life-threatening lower gastrointestinal hemorrhage in an infant after serial transverse enteroplasty: treatment with transcatheter n-butyl-2-cyanoacrylate embolization. Bogue CO, Alzahrani AI, Wales PW, John PR, Amaral JG. Pediatr Radiol. 2009;39(10):1098-101. |
| Gastrointestinal hemorrhage | ||
| Catheterization Digestive System Surgical Procedures Embolization, Therapeutic Enbucrilate Gastrointestinal Hemorrhage Homo sapiens Infant Lower Gastrointestinal Tract Male Radiography, Interventional | ||
| 6 (26.6%) |
19097872 |
[Intestinal obstruction in children due to isolated intestinal malrotation. Report of 11 cases]. Ramirez R, Chaumoitre K, Michel F, Sabiani F, Merrot T. Arch Pediatr. 2009;16(2):99-105. |
| Weight loss Vomiting Melena | ||
| Child Child, Preschool Females Homo sapiens Infant Infant, Newborn Intestinal Obstruction Intestinal Volvulus Male Melena Retrospective Studies Vomiting | ||
| 8 (25.8%) |
30002138 |
Rectal Levothyroxine for the Treatment of Hypothyroidism: A Case Study. Ybarra M, Dos Santos TJ, Pinheiro CTC, Dichtchekenian V, Damiani D. Pediatrics. 2018;142(2):. |
| Hypothyroidism Jaundice | ||
| Child, Preschool Homo sapiens Hypothyroidism Infant Male | ||
| 8 (25.8%) |
16418964 |
Gastroschisis and biliary atresia in a neonate: uncommon presentation or common precipitant. Lee TC, Barshes NR, Nguyen L, Karpen SJ, Quiros-Tejeira RE, Carter BA, Goss JA. Eur J Pediatr Surg. 2005;15(6):434-6. |
| Jaundice | ||
| Biliary Atresia Fatal Outcome Females Gastroschisis Homo sapiens Infant, Newborn | ||
| 8 (25.8%) |
15790327 |
Anterior abdominal wall defects and biliary obstruction. Teoh L, Wong CK, Martin H, O'Loughlin EV. J Paediatr Child Health. 2005;41(3):143-6. |
| Jaundice | ||
| Cholangiography Cholestasis Gastroschisis Homo sapiens Infant, Newborn Jaundice, Obstructive Male |
Total: 3
| HPO ID | Term | Frequency |
|---|---|---|
| HP:0001543 | Gastroschisis | Very frequent (99-80%) |
| HP:0011100 | Intestinal atresia | Frequent (79-30%) |
| HP:0100016 | Abnormality of mesentery morphology | Occasional (29-5%) |
Total: 84
| HPO ID | Term | # of case reports |
|---|---|---|
| HP:0010866 | Abdominal wall defect | 43 |
| HP:0011100 | Intestinal atresia | 20 |
| HP:0004387 | Enterocolitis | 6 |
| HP:0001562 | Oligohydramnios | 5 |
| HP:0002089 | Pulmonary hypoplasia | 5 |
| HP:0002617 | Dilatation | 5 |
| HP:0011102 | Ileal atresia | 5 |
| HP:0100790 | Hernia | 5 |
| HP:0002580 | Volvulus | 4 |
| HP:0000126 | Hydronephrosis | 3 |
| HP:0000952 | Jaundice | 3 |
| HP:0001196 | Short umbilical cord | 3 |
| HP:0001537 | Umbilical hernia | 3 |
| HP:0005214 | Intestinal obstruction | 3 |
| HP:0000822 | Hypertension | 2 |
| HP:0002027 | Abdominal pain | 2 |
| HP:0002098 | Respiratory distress | 2 |
| HP:0002650 | Scoliosis | 2 |
| HP:0002751 | Kyphoscoliosis | 2 |
| HP:0002835 | Aspiration | 2 |
| HP:0002878 | Respiratory failure | 2 |
| HP:0003634 | Amyoplasia | 2 |
| HP:0005912 | Biliary atresia | 2 |
| HP:0031864 | Bacteremia | 2 |
| HP:0100806 | Sepsis | 2 |
| HP:0000028 | Cryptorchidism | 1 |
| HP:0000029 | Testicular atrophy | 1 |
| HP:0000093 | Proteinuria | 1 |
| HP:0000141 | Amenorrhea | 1 |
| HP:0000238 | Hydrocephalus | 1 |
| HP:0000252 | Microcephaly | 1 |
| HP:0000316 | Hypertelorism | 1 |
| HP:0000528 | Anophthalmia | 1 |
| HP:0000541 | Retinal detachment | 1 |
| HP:0000568 | Microphthalmia | 1 |
| HP:0000586 | Shallow orbits | 1 |
| HP:0000609 | Optic nerve hypoplasia | 1 |
| HP:0001156 | Brachydactyly | 1 |
| HP:0001287 | Meningitis | 1 |
| HP:0001321 | Cerebellar hypoplasia | 1 |
| HP:0001371 | Flexion contracture | 1 |
| HP:0001394 | Cirrhosis | 1 |
| HP:0001511 | Intrauterine growth retardation | 1 |
| HP:0001518 | Small for gestational age | 1 |
| HP:0001541 | Ascites | 1 |
| HP:0001558 | Decreased fetal movement | 1 |
| HP:0001622 | Premature birth | 1 |
| HP:0001629 | Ventricular septal defect | 1 |
| HP:0001762 | Talipes equinovarus | 1 |
| HP:0001873 | Thrombocytopenia | 1 |
| HP:0001903 | Anemia | 1 |
| HP:0002021 | Pyloric stenosis | 1 |
| HP:0002139 | Arrhinencephaly | 1 |
| HP:0002315 | Headache | 1 |
| HP:0002435 | Meningocele | 1 |
| HP:0002566 | Intestinal malrotation | 1 |
| HP:0002583 | Colitis | 1 |
| HP:0002612 | Congenital hepatic fibrosis | 1 |
| HP:0002803 | Congenital contracture | 1 |
| HP:0002861 | Melanoma | 1 |
| HP:0002933 | Ventral hernia | 1 |
| HP:0004388 | Microcolon | 1 |
| HP:0004755 | Supraventricular tachycardia | 1 |
| HP:0004756 | Ventricular tachycardia | 1 |
| HP:0004947 | Arteriovenous fistula | 1 |
| HP:0005984 | Elevated maternal serum alpha-fetoprotein | 1 |
| HP:0007209 | Facial paralysis | 1 |
| HP:0008846 | Severe intrauterine growth retardation | 1 |
| HP:0010310 | Chylothorax | 1 |
| HP:0011416 | Placental infarction | 1 |
| HP:0012741 | Unilateral cryptorchidism | 1 |
| HP:0012870 | Vanishing testis | 1 |
| HP:0020110 | Bone fracture | 1 |
| HP:0025023 | Rectal atresia | 1 |
| HP:0025116 | Fetal distress | 1 |
| HP:0030656 | Umbilical vein varix | 1 |
| HP:0030716 | Acrania | 1 |
| HP:0030728 | Meromelia | 1 |
| HP:0030769 | Exencephaly | 1 |
| HP:0031273 | Shock | 1 |
| HP:0100548 | Exstrophy | 1 |
| HP:0100656 | Thoracoabdominal wall defect | 1 |
| HP:0100699 | Scarring | 1 |
| HP:0200133 | Lumbosacral meningocele | 1 |
Total: 0
| Gene Symbol | Gene Name | Entrez Gene ID |
|---|