Rank (Similarity) |
PMID (PMCID) |
---|
|
Total: 13
HPO ID | Term | Frequency |
---|---|---|
HP:0000066 | Labial hypoplasia | Very frequent (99-80%) |
HP:0000252 | Microcephaly | Very frequent (99-80%) |
HP:0000767 | Pectus excavatum | Very frequent (99-80%) |
HP:0001511 | Intrauterine growth retardation | Very frequent (99-80%) |
HP:0001762 | Talipes equinovarus | Very frequent (99-80%) |
HP:0001885 | Short 2nd toe | Very frequent (99-80%) |
HP:0002827 | Hip dislocation | Very frequent (99-80%) |
HP:0003065 | Patellar hypoplasia | Very frequent (99-80%) |
HP:0004322 | Short stature | Very frequent (99-80%) |
HP:0004634 | Cuboid-shaped vertebral bodies | Very frequent (99-80%) |
HP:0005643 | Short 3rd toe | Very frequent (99-80%) |
HP:0011917 | Short 5th toe | Very frequent (99-80%) |
HP:0100490 | Camptodactyly of finger | Very frequent (99-80%) |
Total: 0
HPO ID | Term | # of case reports |
---|
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|