osteogenesis imperfecta type 7
osteogenesis imperfecta that has material basis in mutation in the CRTAP gene on chromosome 3p22
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osteogenesis imperfecta type 7
Summary
osteogenesis imperfecta type 7 is a rare disease[1]. It is known by 8 alternative names across languages and contexts.[2]
Key Facts
- osteogenesis imperfecta type 7's instance of is recorded as rare disease[3].
- osteogenesis imperfecta type 7's instance of is recorded as class of disease[4].
- osteogenesis imperfecta type 7 is a type of osteogenesis imperfecta[5].
- osteogenesis imperfecta type 7 is a type of genetic disease[6].
- osteogenesis imperfecta type 7 is a type of autosomal recessive disease[7].
- osteogenesis imperfecta type 7's health specialty is recorded as medical genetics[8].
- osteogenesis imperfecta type 7's genetic association is recorded as CRTAP[9].
- osteogenesis imperfecta type 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110337[10].
- osteogenesis imperfecta type 7's exact match is recorded as http://identifiers.org/doid/DOID:0110337[11].
- osteogenesis imperfecta type 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
osteogenesis imperfecta type 7 is known by 8 alternative names across languages and contexts.[2]