osteogenesis imperfecta type 9
osteogenesis imperfecta that has material basis in mutation in the PPIB gene on chromosome 15q22
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osteogenesis imperfecta type 9
Summary
osteogenesis imperfecta type 9 is a developmental defect during embryogenesis[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- osteogenesis imperfecta type 9's instance of is recorded as developmental defect during embryogenesis[3].
- osteogenesis imperfecta type 9's instance of is recorded as rare disease[4].
- osteogenesis imperfecta type 9's instance of is recorded as class of disease[5].
- osteogenesis imperfecta type 9 is a type of osteogenesis imperfecta[6].
- osteogenesis imperfecta type 9 is a type of genetic disease[7].
- osteogenesis imperfecta type 9 is a type of autosomal recessive disease[8].
- osteogenesis imperfecta type 9's health specialty is recorded as medical genetics[9].
- osteogenesis imperfecta type 9's genetic association is recorded as PPIB[10].
- osteogenesis imperfecta type 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110349[11].
- osteogenesis imperfecta type 9's exact match is recorded as http://identifiers.org/doid/DOID:0110349[12].
- osteogenesis imperfecta type 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
osteogenesis imperfecta type 9 is known by 6 alternative names across languages and contexts.[2]