Concept information
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Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
...
Disease of the musculoskeletal system, NOS
Congenital anomaly of musculoskeletal system
Skeletal dysplasia
Osteogenesis imperfecta
...
Disease of the musculoskeletal system, NOS
Congenital anomaly of musculoskeletal system
Skeletal dysplasia
Osteogenesis imperfecta
...
Congenital malformation
Congenital anomaly of musculoskeletal system
Skeletal dysplasia
Osteogenesis imperfecta
...
Congenital malformation
Congenital anomaly of musculoskeletal system
Skeletal dysplasia
Osteogenesis imperfecta
...
Disease of the musculoskeletal system, NOS
Congenital anomaly of musculoskeletal system
Congenital anomaly of skeletal bone
Osteogenesis imperfecta
...
Disease of the musculoskeletal system, NOS
Congenital anomaly of musculoskeletal system
Congenital anomaly of skeletal bone
Osteogenesis imperfecta
Preferred term
Osteogenesis imperfecta type I (disorder)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
Associated morphology
Finding site
Has interpretation
Interprets
Is a
- 363070008
- 363212003
- Dominant hereditary disorder, NOS
- Osteogenesis imperfecta
Occurrence
Pathological process
In other languages
URI
http://www.irandoc.acir/onto/irandoc/385482004
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