Mondo Disease Ontology
5883 terms(s) returned
| Term Type: | Record: 2001 to 2050 of 5883 Records | Page: 41 of 118, First Previous Next Last | Show Records Per Page |
- patched1-related cardiovascular disorder, Nile tilapia
- patella
- patella aplasia/hypoplasia
- patella aplasia/hypoplasia, bilateral
- patella aplasia/hypoplasia, unilateral
- patella cartilage element
- patella pre-cartilage condensation
- patella, familial recurrent dislocation of
- patellar fracture and dental anomaly syndrome, domestic cat
- patellar luxation, non-human animal
- patellar osteochondritis dissecans, non-human animal
- patellar tendinitis
- patellofemoral joint
- patellofemoral pain syndrome
- patent ductus arteriosus
- patent ductus arteriosus 2
- patent ductus arteriosus 3
- patent ductus arteriosus with left-to-right shunt, non-human animal
- patent ductus arteriosus with right-to-left shunt, non-human animal
- patent ductus arteriosus, cattle
- patent ductus arteriosus, chicken
- patent ductus arteriosus, dog
- patent ductus arteriosus, domestic cat
- patent ductus arteriosus, horse
- patent ductus arteriosus, non-human animal
- patent ductus arteriosus, sheep
- patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome
- patent ductus venosus
- patent ductus venosus, dog
- patent ductus venosus, gray wolf
- patent ductus venosus, non-human animal
- patent foramen ovale
- patent foramen ovale, non-human animal
- patent urachus
- patent urachus, dog
- patent urachus, domestic cat
- patent urachus, mountain zebra
- patent urachus, non-human animal
- patent urachus, sheep
- patent urachus, white rhinoceros
- paternal 14q32.2 hypomethylation syndrome
- paternal 14q32.2 microdeletion syndrome
- paternal 20q13.2q13.3 microdeletion syndrome
- paternal uniparental disomy of chromosome 1
- paternal uniparental disomy of chromosome 13
- paternal uniparental disomy of chromosome 14
- paternal uniparental disomy of chromosome 20
- paternal uniparental disomy of chromosome 21
- paternal uniparental disomy of chromosome 5
- paternal uniparental disomy of chromosome 6
