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2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Other Congenital Musculoskeletal Anomalies 756.* >

2007 ICD-9-CM Diagnosis 756.59

Other congenital osteodystrophies

This code may be outdated. View 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

756.59 also known as:

  • Albright (-McCune)-Sternberg syndrome

Index entries containing 756.59:

Aclasis
  • tarsoepiphyseal 756.59
Acromicria, acromikria 756.59
Albright (-McCune) (-Sternberg) syndrome (osteitis fibrosa disseminata) 756.59
Caffey's disease or syndrome (infantile cortical hyperostosis) 756.59
Camurati-Engelmann disease (diaphyseal sclerosis) 756.59
Chondroangiopathia calcarea seu punctate 756.59
Chondrodysplasia 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) 756.59
Disease, 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 756.59
Dysplasia - 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) 756.59
Fibrosis, fibrotic
  • bone, diffuse 756.59
Fuller Albright's syndrome (osteitis fibrosa disseminata) 756.59
Hyperostosis 733.99
  • cortical 733.3
    • infantile 756.59
Léri-Weill syndrome 756.59
McCune-Albright syndrome (osteitis fibrosa disseminata) 756.59
Osteitis (see also Osteomyelitis) 730.2
  • fibrosa NEC 733.29
    • disseminata 756.59
Osteochondritis (see also Osteochondrosis) 732.9
  • multiple 756.59
Osteochondrodermodysplasia 756.59
Osteodystrophy
  • congenital 756.50
    • specified type NEC 756.59
Osteopathia
  • hyperostotica multiplex infantilis 756.59
Ostrum-Furst syndrome 756.59
Periostosis (see also Periostitis) 730.3
  • hyperplastic 756.59
Stippled epiphyses 756.59
Syndrome - 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