| Rank (Similarity) |
PMID (PMCID) |
|
|---|---|---|
| 30 (4.0%) |
4003443 |
Ectopia cordis and cleft sternum: evidence for mechanical teratogenesis following rupture of the chorion or yolk sac. Kaplan LC, Matsuoka R, Gilbert EF, Opitz JM, Kurnit DM. Am J Med Genet. 1985;21(1):187-202. |
| Pulmonary hypoplasia | ||
| Amniotic Band Syndrome Chorion Congenital Heart Defects Females Homo sapiens Infant, Newborn Pregnancy Sternum Yolk Sac | ||
| 30 (4.0%) |
3537999 |
Trisomy 18 with ectopia cordis, omphalocele, and ventricular septal defect: case report. Soper SP, Roe LR, Hoyme HE, Clemmons JJ. Pediatr Pathol. 1986;5(3-4):481-3. |
| Ventricular septal defect | ||
| Chromosome Mapping Chromosomes, Human, Pair 18 Congenital Heart Defects Gestational Age Homo sapiens Male Trisomy Ultrasonography Ventricular Septal Defects | ||
| 30 (4.0%) |
3232702 |
Trisomy 18 with Cantrell pentalogy in a stillborn infant. Fox JE, Gloster ES, Mirchandani R. Am J Med Genet. 1988;31(2):391-4. |
| Horseshoe kidney | ||
| Chromosomes, Human, Pair 18 Females Fetal Death Homo sapiens Infant, Newborn Pregnancy Trisomy | ||
| 30 (4.0%) |
3189399 |
Trisomy 18 associated with ectopia cordis and occipital meningocele. Bick D, Markowitz RI, Horwich A. Am J Med Genet. 1988;30(3):805-10. |
| Occipital meningocele | ||
| Chromosomes, Human, Pair 18 Congenital Heart Defects Females Homo sapiens Infant, Newborn Trisomy | ||
| 30 (4.0%) |
2732539 |
[Thoracoabdominal ectopia cordis with single ventricle and pulmonary stenosis. A case report of successful surgical repair]. Tachibana H, Gan K, Oshima Y, Ohashi H, Hosokawa Y, Yamaguchi M. Nihon Kyobu Geka Gakkai Zasshi. 1989;37(1):148-53. |
| Cyanosis | ||
| Child Congenital Heart Defects Heart Ventricle Homo sapiens Male Pulmonary Valve Stenosis | ||
| 30 (4.0%) |
2063890 |
New multiple congenital anomalies syndrome in a stillborn infant of consanguinous parents and a prediabetic pregnancy. Van Allen MI, Myhre S. Am J Med Genet. 1991;38(4):523-8. |
| Obesity | ||
| Adult Chromosome Aberrations Females Fetal Death Genes, Recessive Homo sapiens Infant, Newborn Pregnancy Pregnancy in Diabetics | ||
| 30 (4.0%) |
1828812 |
Diffuse neonatal hemangiomatosis: a new constellation of findings. Geller JD, Topper SF, Hashimoto K. J Am Acad Dermatol. 1991;24(5 Pt 2):816-8. |
| Visceral hemangioma | ||
| Abdominal Muscles Congenital Heart Defects Hemangioma Homo sapiens Infant, Newborn Male Neoplasms, Multiple Primary Skin Neoplasms | ||
| 30 (4.0%) |
1728225 |
Complete thoracic ectopia cordis with double-outlet right ventricle: neonatal repair. Watterson KG, Wilkinson JL, Kliman L, Mee RB. Ann Thorac Surg. 1992;53(1):146-7. |
| Ventricular septal defect | ||
| Congenital Heart Defects Double Outlet Right Ventricle Homo sapiens Infant, Newborn Male Sternum Ventricular Septal Defects | ||
| 30 (4.0%) |
1492509 |
Cardiac function, morphology and chromosomal aberrations in a calf with ectopia cordis cervicalis. Windberger U, Forstenpointner G, Grabenwoger F, Kopp E, Kunzel W, Mayr B, Pernthaner A, Simon P, Losert U. Zentralbl Veterinarmed A. 1992;39(10):759-68. |
| Hypertension | ||
| Animals Cattle Cattle Diseases Chromosome Aberrations Congenital Heart Defects Heart Male Myocardium | ||
| 30 (4.0%) |
159022 |
Immediate operation for ectopia cordis. Jones AF, McGrath RL, Edwards SM, Lilly JR. Ann Thorac Surg. 1979;28(5):484-6. |
| Abdominal wall defect | ||
| Abdominal Muscles Age Factors Congenital Heart Defects Homo sapiens Infant, Newborn Male Methods Prostheses and Implants Silicone Elastomers Surgical Flaps Surgical Mesh Ventricular Septal Defects |
Total: 0
| HPO ID | Term | Frequency |
|---|
Total: 34
| HPO ID | Term | # of case reports |
|---|---|---|
| HP:0010866 | Abdominal wall defect | 13 |
| HP:0001629 | Ventricular septal defect | 5 |
| HP:0001750 | Single ventricle | 4 |
| HP:0010309 | Bifid sternum | 3 |
| HP:0100790 | Hernia | 3 |
| HP:0000476 | Cystic hygroma | 2 |
| HP:0000528 | Anophthalmia | 2 |
| HP:0100656 | Thoracoabdominal wall defect | 2 |
| HP:0000141 | Amenorrhea | 1 |
| HP:0000238 | Hydrocephalus | 1 |
| HP:0000252 | Microcephaly | 1 |
| HP:0000316 | Hypertelorism | 1 |
| HP:0000347 | Micrognathia | 1 |
| HP:0000369 | Low-set ears | 1 |
| HP:0000568 | Microphthalmia | 1 |
| HP:0000879 | Short sternum | 1 |
| HP:0001028 | Hemangioma | 1 |
| HP:0001528 | Hemihypertrophy | 1 |
| HP:0001561 | Polyhydramnios | 1 |
| HP:0001746 | Asplenia | 1 |
| HP:0002323 | Anencephaly | 1 |
| HP:0002436 | Occipital meningocele | 1 |
| HP:0002650 | Scoliosis | 1 |
| HP:0002825 | Caudal appendage | 1 |
| HP:0005160 | Total anomalous pulmonary venous return | 1 |
| HP:0008070 | Sparse hair | 1 |
| HP:0009829 | Phocomelia | 1 |
| HP:0010301 | Spinal dysraphism | 1 |
| HP:0011565 | Common atrium | 1 |
| HP:0011623 | Muscular ventricular septal defect | 1 |
| HP:0030754 | Allantoic cyst | 1 |
| HP:0030769 | Exencephaly | 1 |
| HP:0031046 | Absent soft palate | 1 |
| HP:0100336 | Bilateral cleft lip | 1 |
Total: 0
| Gene Symbol | Gene Name | Entrez Gene ID |
|---|