| Rank (Similarity) |
PMID (PMCID) |
|
|---|---|---|
| 6 (4.0%) |
3290573 |
[Embryopathy and diabetic fetopathy in a premature stillborn infant. Case report and review of the disease picture]. Schwaibold H, Wittekind C, Schillinger H, Bohm N. Klin Padiatr. 1988;200(2):135-9. |
| Obesity | ||
| Autopsy Diabetes Mellitus, Insulin-Dependent Females Fetal Death Homo sapiens Pregnancy Pregnancy in Diabetics Syndrome Ultrasonography | ||
| 6 (4.0%) |
2260569 |
Acrofacial dysostosis with ambiguous genitalia. Wulfsberg EA, Curtis J, Wiswell TE, Puntel RA, Levin SW. Am J Med Genet. 1990;37(3):384-7. |
| Ambiguous genitalia | ||
| Craniofacial Dysostosis Homo sapiens Infant, Newborn Male Male Genital Organs Syndrome | ||
| 6 (4.0%) |
2028782 |
Unique brain anomalies in an infant of a diabetic mother. Kousseff BG, Villaveces C, Martinez CR. Acta Paediatr Scand. 1991;80(1):110-5. |
| Megacystis | ||
| NGF | ||
| Adult Brain Females Homo sapiens Infant, Newborn Pregnancy Pregnancy in Diabetics |
Total: 32
| HPO ID | Term | Frequency |
|---|---|---|
| HP:0000008 | Abnormality of female internal genitalia | Very frequent (99-80%) |
| HP:0000028 | Cryptorchidism | Very frequent (99-80%) |
| HP:0000054 | Micropenis | Very frequent (99-80%) |
| HP:0000073 | Ureteral duplication | Very frequent (99-80%) |
| HP:0000126 | Hydronephrosis | Very frequent (99-80%) |
| HP:0000175 | Cleft palate | Very frequent (99-80%) |
| HP:0000252 | Microcephaly | Very frequent (99-80%) |
| HP:0000368 | Low-set, posteriorly rotated ears | Very frequent (99-80%) |
| HP:0000464 | Abnormality of the neck | Very frequent (99-80%) |
| HP:0001629 | Ventricular septal defect | Very frequent (99-80%) |
| HP:0001636 | Tetralogy of Fallot | Very frequent (99-80%) |
| HP:0001669 | Transposition of the great arteries | Very frequent (99-80%) |
| HP:0001679 | Abnormal aortic morphology | Very frequent (99-80%) |
| HP:0002564 | obsolete Malformation of the heart and great vessels | Very frequent (99-80%) |
| HP:0003422 | Vertebral segmentation defect | Very frequent (99-80%) |
| HP:0004414 | Abnormality of the pulmonary artery | Very frequent (99-80%) |
| HP:0005107 | Abnormal sacrum morphology | Very frequent (99-80%) |
| HP:0008056 | Aplasia/Hypoplasia affecting the eye | Very frequent (99-80%) |
| HP:0008551 | Microtia | Very frequent (99-80%) |
| HP:0008678 | Renal hypoplasia/aplasia | Very frequent (99-80%) |
| HP:0010318 | Aplasia/Hypoplasia of the abdominal wall musculature | Very frequent (99-80%) |
| HP:0000098 | Tall stature | Frequent (79-30%) |
| HP:0000238 | Hydrocephalus | Frequent (79-30%) |
| HP:0000347 | Micrognathia | Frequent (79-30%) |
| HP:0000365 | Hearing impairment | Frequent (79-30%) |
| HP:0000707 | Abnormality of the nervous system | Frequent (79-30%) |
| HP:0001195 | Single umbilical artery | Frequent (79-30%) |
| HP:0002007 | Frontal bossing | Frequent (79-30%) |
| HP:0007360 | Aplasia/Hypoplasia of the cerebellum | Frequent (79-30%) |
| HP:0007370 | Aplasia/Hypoplasia of the corpus callosum | Frequent (79-30%) |
| HP:0010301 | Spinal dysraphism | Frequent (79-30%) |
| HP:0001732 | Abnormality of the pancreas | Occasional (29-5%) |
Total: 7
| HPO ID | Term | # of case reports |
|---|---|---|
| HP:0010442 | Polydactyly | 2 |
| HP:0000021 | Megacystis | 1 |
| HP:0000072 | Hydroureter | 1 |
| HP:0000819 | Diabetes mellitus | 1 |
| HP:0001622 | Premature birth | 1 |
| HP:0003097 | Short femur | 1 |
| HP:0009800 | Maternal diabetes | 1 |
Total: 0
| Gene Symbol | Gene Name | Entrez Gene ID |
|---|