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Fibrös skeletal dysplasi
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Anmärkning: | A disease of bone marked by thinning of the cortex and replacement of bone marrow by gritty fibrous tissue containing bony spicules, producing pain, disability, and gradually increasing deformity. Only one bone may be involved (FIBROUS DYSPLASIA, MONOSTOTIC) or several (FIBROUS DYSPLASIA, POLYOSTOTIC). (From Dorland, 28th ed)
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Annotation: | GEN or unspecified; prefer specifics; periapical fibrous dysplasia = CEMENTOMA; craniofacial fibrous dysplasia = FIBROUS DYSPLASIA, POLYOSTOTIC (IM) + SKULL (IM) + FACIAL BONES (IM)
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historyNote*: | 67; was FIBROUS DYSPLASIA 1963-66 (Prov); ALBRIGHT'S DISEASE & JAFFE-LICHTENSTEIN DISEASE were see under OSTEITIS FIBROSA 1963-66
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onlineNote*: | use FIBROUS DYSPLASIA OF BONE to search FIBROUS DYSPLASIA 1966 (as Prov); search ALBRIGHT'S DISEASE & JAFFE-LICHTENSTEIN DISEASE under OSTEITIS FIBROSA CYSTICA 1966
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publicMeSHNote*: | 67; ALBRIGHT'S DISEASE & JAFFE-LICHTENSTEIN DISEASE were see under OSTEITIS FIBROSA 1963-66
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dateCreated*: | 1999-01-01X |
dateEstablished*: | 1967-01-01X |
dateRevised*: | 1996-06-10X |
recordAuthorizer*: | PLSX |
recordMaintainer*: | TGCX |
recordOriginator*: | NLMX |
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Termer och motsvarande begrepp: | Luun fibroottinen dysplasia (fi) XFibroottinen dysplasia (fi, ersatt) Fibrous Dysplasia of Bone (en) Osteitis Fibrosa Disseminata (en, ersatt) Dysplasia fibrotica (la-FI, ersatt) |
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