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The way concept relations are shown:
Osteogenesis Imperfecta
Hierarchy: | ∟ ∟ ∟ Osteogenesis Imperfecta 53 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Keloid | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ CADASIL | ∟ ∟ ∟ ∟ ∟ Dwarfism | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Osteogenesis Imperfecta 53 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Keloid | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ CADASIL | ∟ ∟ ∟ ∟ ∟ Dwarfism | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Osteogenesis Imperfecta 53 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Keloid | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ CADASIL | ∟ ∟ ∟ ∟ ∟ Dwarfism | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
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Scope note: | Autosomal dominant COLLAGEN DISEASES resulting from defective biosynthesis of COLLAGEN TYPE I and characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. There are four major types, I-IV.
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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Synnynnäinen luutumisvajaus (fi, replaced) XLobstein Disease (en, replaced) Fragilitas Ossium (en, replaced) |
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