Mondo Disease Ontology
5419 terms(s) returned
Term Type: | Record: 5101 to 5150 of 5419 Records | Page: 103 of 109, First Previous Next Last | Show Records Per Page |
- osteogenesis imperfecta type 7
- osteogenesis imperfecta type 8
- osteogenesis imperfecta type 9
- osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
- osteogenesis imperfecta, IIA 22
- osteogenesis imperfecta, cattle
- osteogenesis imperfecta, dog
- osteogenesis imperfecta, domestic cat
- osteogenesis imperfecta, non-human animal
- osteogenesis imperfecta, sheep
- osteogenesis imperfecta, type 18
- osteogenesis imperfecta, type 19
- osteogenesis imperfecta, type 20
- osteogenesis imperfecta, type 21
- osteogenesis imperfecta, type 23
- osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome
- osteogenic neoplasm
- osteoglophonic dwarfism
- osteoid
- osteoid osteoma
- osteoma
- osteoma of cranial vault, familial
- osteoma of middle ear
- osteomalacia
- osteomas of mandible
- osteomesopyknosis
- osteomyelitis
- osteonecrosis
- osteonecrosis of genetic origin
- osteonecrosis of the jaw
- osteootohepatoenteric syndrome
- osteopathia striata with cranial sclerosis
- osteopathia striata-pigmentary dermopathy-white forelock syndrome
- osteopenia-intellectual disability-sparse hair syndrome
- osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome
- osteopetrosis
- osteopetrosis with gingival hamartomas, cattle
- osteopetrosis with gingival hamartomas, non-human animal
- osteopetrosis, Japanese quail
- osteopetrosis, ass
- osteopetrosis, autosomal dominant 3
- osteopetrosis, autosomal recessive 9
- osteopetrosis, cattle
- osteopetrosis, horse
- osteopetrosis, non-human animal
- osteopetrosis, rabbit
- osteopoikilosis
- osteoporosis
- osteoporosis, childhood- or juvenile-onset, with developmental delay
- osteoporosis, horse