Rank (Similarity) |
PMID (PMCID) |
---|
|
Total: 19
HPO ID | Term | Frequency |
---|---|---|
HP:0000175 | Cleft palate | Very frequent (99-80%) |
HP:0000252 | Microcephaly | Very frequent (99-80%) |
HP:0000400 | Macrotia | Very frequent (99-80%) |
HP:0002750 | Delayed skeletal maturation | Very frequent (99-80%) |
HP:0004322 | Short stature | Very frequent (99-80%) |
HP:0000047 | Hypospadias | Frequent (79-30%) |
HP:0000212 | Gingival overgrowth | Frequent (79-30%) |
HP:0000347 | Micrognathia | Frequent (79-30%) |
HP:0000411 | Protruding ear | Frequent (79-30%) |
HP:0000508 | Ptosis | Frequent (79-30%) |
HP:0000767 | Pectus excavatum | Frequent (79-30%) |
HP:0001252 | Muscular hypotonia | Frequent (79-30%) |
HP:0001263 | Global developmental delay | Frequent (79-30%) |
HP:0001800 | Hypoplastic toenails | Frequent (79-30%) |
HP:0003202 | Skeletal muscle atrophy | Frequent (79-30%) |
HP:0004428 | Elfin facies | Frequent (79-30%) |
HP:0006709 | Aplasia/Hypoplasia of the nipples | Frequent (79-30%) |
HP:0009465 | Ulnar deviation of finger | Frequent (79-30%) |
HP:0009882 | Short distal phalanx of finger | Frequent (79-30%) |
Total: 0
HPO ID | Term | # of case reports |
---|
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|