Rank (Similarity) |
PMID (PMCID) |
|
---|---|---|
1 (52.1%) |
23607868 |
A case of dichorionic twin pregnancy concordant for bilateral cleft lip and palate and discordant for spina bifida; schisis association. Kutuk MS, Ozgun MT, Uludag S, Akgun H, Balta B. Fetal Pediatr Pathol. 2013;32(5):371-4. |
Oral cleft Oligodactyly | ||
Cleft Palate Diseases in Twins Females Homo sapiens Male Pregnancy Spina Bifida Toes Young Adult | ||
2 (39.0%) |
12116204 |
Developmental field defects: coming together of associations and sequences during blastogenesis. Hersh JH, Angle B, Fox TL, Barth RF, Bendon RW, Gowans G. Am J Med Genet. 2002;110(4):320-3. |
Encephalocele | ||
Anus, Imperforate Chromosome Aberrations Chromosomes, Human, Pair 18 Congenital Heart Defects Ectromelia Fatal Outcome Fetal Diseases Holoprosencephaly Homo sapiens Infant, Newborn Kidney Male | ||
3 (34.6%) |
8074153 |
Split hand/split foot, syndactyly, urinary tract obstruction, radial, diaphragmatic, and neural tube defects: Czeizel-Losonci syndrome? Genuardi M, Silvestri E, Tozzi C. Am J Med Genet. 1994;51(3):247-50. |
Hydronephrosis Syndactyly Split hand | ||
Fatal Outcome Females Genes, Dominant Homo sapiens Hydronephrosis Infant, Newborn Limb Deformities, Congenital Neural Tube Defects Respiratory Diaphragm Syndactyly Syndrome |
Total: 15
HPO ID | Term | Frequency |
---|---|---|
HP:0000175 | Cleft palate | Very frequent (99-80%) |
HP:0001518 | Small for gestational age | Very frequent (99-80%) |
HP:0001539 | Omphalocele | Very frequent (99-80%) |
HP:0001622 | Premature birth | Very frequent (99-80%) |
HP:0002323 | Anencephaly | Very frequent (99-80%) |
HP:0100333 | Unilateral cleft lip | Very frequent (99-80%) |
HP:0000776 | Congenital diaphragmatic hernia | Frequent (79-30%) |
HP:0002084 | Encephalocele | Frequent (79-30%) |
HP:0002414 | Spina bifida | Frequent (79-30%) |
HP:0000104 | Renal agenesis | Occasional (29-5%) |
HP:0000252 | Microcephaly | Occasional (29-5%) |
HP:0002023 | Anal atresia | Occasional (29-5%) |
HP:0002564 | obsolete Malformation of the heart and great vessels | Occasional (29-5%) |
HP:0002575 | Tracheoesophageal fistula | Occasional (29-5%) |
HP:0002983 | Micromelia | Occasional (29-5%) |
Total: 2
HPO ID | Term | # of case reports |
---|---|---|
HP:0002084 | Encephalocele | 1 |
HP:0002414 | Spina bifida | 1 |
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|