Rank (Similarity) |
PMID (PMCID) |
---|
|
Total: 17
HPO ID | Term | Frequency |
---|---|---|
HP:0000028 | Cryptorchidism | Very frequent (99-80%) |
HP:0000079 | Abnormality of the urinary system | Very frequent (99-80%) |
HP:0000235 | Abnormality of the fontanelles or cranial sutures | Very frequent (99-80%) |
HP:0000256 | Macrocephaly | Very frequent (99-80%) |
HP:0000286 | Epicanthus | Very frequent (99-80%) |
HP:0000316 | Hypertelorism | Very frequent (99-80%) |
HP:0000343 | Long philtrum | Very frequent (99-80%) |
HP:0000431 | Wide nasal bridge | Very frequent (99-80%) |
HP:0000463 | Anteverted nares | Very frequent (99-80%) |
HP:0000470 | Short neck | Very frequent (99-80%) |
HP:0000774 | Narrow chest | Very frequent (99-80%) |
HP:0001155 | Abnormality of the hand | Very frequent (99-80%) |
HP:0001252 | Muscular hypotonia | Very frequent (99-80%) |
HP:0001274 | Agenesis of corpus callosum | Very frequent (99-80%) |
HP:0001387 | Joint stiffness | Very frequent (99-80%) |
HP:0006610 | Wide intermamillary distance | Very frequent (99-80%) |
HP:0008736 | Hypoplasia of penis | Very frequent (99-80%) |
Total: 0
HPO ID | Term | # of case reports |
---|
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|