osteogenesis imperfecta
osteochondrodysplasia that has material basis in a deficiency in type-I collagen which results in brittle bones and defective connective tissue
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osteogenesis imperfecta
Summary
osteogenesis imperfecta is a designated intractable/rare disease[1]. It has Wikipedia articles in 26 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- osteogenesis imperfecta's instance of is recorded as designated intractable/rare disease[3].
- osteogenesis imperfecta's instance of is recorded as rare disease[4].
- osteogenesis imperfecta's instance of is recorded as class of disease[5].
- osteogenesis imperfecta is a type of osteochondrodysplasia[6].
- osteogenesis imperfecta is a type of disease[7].
- osteogenesis imperfecta's Commons category is recorded as Osteogenesis imperfecta[8].
- osteogenesis imperfecta's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4567[9].
- osteogenesis imperfecta's ICD-9-CM is recorded as 756.51[10].
- osteogenesis imperfecta's NCI Thesaurus ID is recorded as C26837[11].
- osteogenesis imperfecta's NCI Thesaurus ID is recorded as C99003[12].
- osteogenesis imperfecta's health specialty is recorded as medical genetics[13].
- osteogenesis imperfecta's genetic association is recorded as COL1A1[14].
- osteogenesis imperfecta's exact match is recorded as http://purl.obolibrary.org/obo/DOID_12347[15].
- osteogenesis imperfecta's exact match is recorded as http://identifiers.org/doid/DOID:12347[16].
- osteogenesis imperfecta's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_666[17].
- osteogenesis imperfecta's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
osteogenesis imperfecta has Wikipedia articles in 26 language editions, a strong signal of global cultural recognition.[2] It is known by 54 alternative names across languages and contexts.[19]