2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Other Congenital Musculoskeletal Anomalies 756.* > 2006 ICD-9-CM Diagnosis 756.59
Other congenital osteodystrophiesView the most recent version of ICD-9-CM 756.59 - 756.59 is a specific code that can be used to specify a diagnosis
- 756.59 contains 49 index entries
- View the ICD-9-CM Volume 1 756.* hierarchy
Alternate Terminology- Albright (-McCune)-Sternberg syndrome
Index entries containing 756.59:
- Aclasis
- tarsoepiphyseal
756.59 Acromicria, acromikria 756.59Albright (-McCune) (-Sternberg) syndrome (osteitis fibrosa disseminata) 756.59Caffey's disease or syndrome (infantile cortical hyperostosis) 756.59Camurati-Engelmann disease (diaphyseal sclerosis) 756.59Chondroangiopathia calcarea seu punctate 756.59Chondrodysplasia 756.4- calcificans congenita
756.59 - epiphysialis punctata
756.59 Chondrodystrophia (fetalis) 756.4- calcificans congenita
756.59 - fetalis hypoplastica
756.59 - hypoplastica calcinosa
756.59 - punctata
756.59 Conradi (-Hünermann) syndrome or disease (chondrodysplasia calcificans congenita) 756.59Disease, diseased - see also Syndrome- caffey's (infantile cortical hyperostosis)
756.59 - Camurati-Engelmann (diaphyseal sclerosis)
756.59 - Conradi (-Hünermann)
756.59 - Engelmann's (diaphyseal sclerosis)
756.59 - Paas'
756.59 Dyschondrosteosis 756.59Dysplasia - see also Anomaly- bone (fibrous) NEC 733.29
- diaphyseal, progressive
756.59
- diaphyseal, progressive
756.59 - epiphysealis 756.9
- punctata
756.59
- fibrous
- diaphyseal, progressive
756.59
- progressive diaphyseal
756.59 Dystrophy, dystrophia 783.9- chondro-osseus with punctate epiphyseal dysplasia
756.59 - familial
- hyperplastic periosteal
756.59
Engelmann's disease (diaphyseal sclerosis) 756.59Fibrosis, fibrotic- bone, diffuse
756.59 Fuller Albright's syndrome (osteitis fibrosa disseminata) 756.59Hyperostosis 733.99- cortical 733.3
- infantile
756.59
Léri-Weill syndrome 756.59McCune-Albright syndrome (osteitis fibrosa disseminata) 756.59Osteitis (see also Osteomyelitis) 730.2- fibrosa NEC 733.29
- disseminata
756.59
Osteochondritis (see also Osteochondrosis) 732.9- multiple
756.59 Osteochondrodermodysplasia 756.59Osteodystrophy- congenital 756.50
- specified type NEC
756.59
Osteopathia- hyperostotica multiplex infantilis
756.59 Ostrum-Furst syndrome 756.59Periostosis (see also Periostitis) 730.3- hyperplastic
756.59 Stippled epiphyses 756.59Syndrome - see also Disease- Albright-McCune-Sternberg (osteitis fibrosa disseminata)
756.59 - brown spot
756.59 - Caffey's (infantile cortical hyperostosis)
756.59 - Conradi (-Hünermann) (chondrodysplasia calcificans congenita)
756.59 - Fuller Albright's (osteitis fibrosa disseminata)
756.59 - Léri-Weill
756.59 - McCune-Albright (osteitis fibrosa disseminata)
756.59 - Ostrum-Furst
756.59 Synostosis (congenital) 756.59
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