Rank (Similarity) |
PMID (PMCID) |
---|
|
Total: 13
HPO ID | Term | Frequency |
---|---|---|
HP:0000703 | Dentinogenesis imperfecta | Very frequent (99-80%) |
HP:0011120 | Concave nasal ridge | Very frequent (99-80%) |
HP:0000268 | Dolichocephaly | Frequent (79-30%) |
HP:0000316 | Hypertelorism | Frequent (79-30%) |
HP:0000629 | Periorbital fullness | Frequent (79-30%) |
HP:0002645 | Wormian bones | Frequent (79-30%) |
HP:0002756 | Pathologic fracture | Frequent (79-30%) |
HP:0003103 | Abnormal cortical bone morphology | Frequent (79-30%) |
HP:0004322 | Short stature | Frequent (79-30%) |
HP:0009824 | Upper limb undergrowth | Frequent (79-30%) |
HP:0001376 | Limitation of joint mobility | Occasional (29-5%) |
HP:0001773 | Short foot | Occasional (29-5%) |
HP:0001863 | Toe clinodactyly | Occasional (29-5%) |
Total: 0
HPO ID | Term | # of case reports |
---|
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|