osteogenesis imperfecta type 17
osteogenesis imperfecta that has material basis in mutation in the SPARC gene on chromosome 5q33
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osteogenesis imperfecta type 17
Summary
osteogenesis imperfecta type 17 is a rare disease[1].
Key Facts
- osteogenesis imperfecta type 17's instance of is recorded as rare disease[2].
- osteogenesis imperfecta type 17's instance of is recorded as class of disease[3].
- osteogenesis imperfecta type 17 is a type of osteogenesis imperfecta[4].
- osteogenesis imperfecta type 17 is a type of genetic disease[5].
- osteogenesis imperfecta type 17 is a type of autosomal recessive disease[6].
- osteogenesis imperfecta type 17's health specialty is recorded as medical genetics[7].
- osteogenesis imperfecta type 17's genetic association is recorded as SPARC[8].
- osteogenesis imperfecta type 17's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110338[9].
- osteogenesis imperfecta type 17's exact match is recorded as http://identifiers.org/doid/DOID:0110338[10].
- osteogenesis imperfecta type 17's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].