Home > 2007 ICD-9-CM Diagnosis Codes > Congenital Anomalies 740-759 > Other congenital musculoskeletal anomalies 756-
Specific code 2007 ICD-9-CM Diagnosis Code 756.59
Other congenital osteodystrophies
  • Short description: OSTEODYSTROPHY NEC.
  • ICD-9-CM 756.59 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 756.59 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
  • You are viewing the 2007 version of ICD-9-CM 756.59.
  • More recent version(s) of ICD-9-CM 756.59: 2008 2009 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM: 756.59 converts approximately to:
  • 2015/16 ICD-10-CM Q78.8 Other specified osteochondrodysplasias
Approximate Synonyms
  • Acrodysostosis
  • Acromicric dysplasia
  • Albright mccune sternberg syndrome
  • Bent bone dysplasia
  • Capitate-hamate synostosis
  • Carpal-tarsal osteolysis with nephropathy
  • Chondrodysplasia punctata
  • Chondrodysplasia punctata (stippled epiphyses) group (disorder)
  • Chondrodysplasia punctata congenita
  • Chondrodysplasia punctata, Conradi-H�nermann type
  • Chondrodysplasia punctata, MT type
  • Chondrodysplasia punctata, X-linked dominant type
  • Chondrodysplasia punctata, X-linked recessive type
  • Craniodiaphyseal dysplasia
  • Dappled diaphyseal dysplasia
  • Diaphyseal dysplasia
  • Diaphyseal dysplasia with anemia
  • Disuse osteodystrophy
  • Dysplasia epiphysealis hemimelica
  • Furst-Ostrum syndrome
  • Hajdu-Cheney syndrome
  • Hepatic osteodystrophy
  • Hyperphosphatasia-osteoectasia syndrome
  • Infantile cortical hyperostosis
  • Kniest-Stickler dysplasia group
  • Langer mesomelic dysplasia syndrome
  • Lenz-Majewski hyperostosis syndrome
  • Leri-Weill dyschondrosteosis
  • Melnick-Needles syndrome
  • Metachondromatosis
  • Omodysplasia I
  • Omodysplasia II
  • Osteochondrodysplasia
  • Polyostotic fibrous dysplasia of bone
  • Progressive diaphyseal dysplasia
  • Rolland-Debuqois syndrome
  • Sclerosteosis
  • Spondyloepiphyseal dysplasia congenita
  • Ulnar and humeroulnar synostosis
  • X-linked dominant chondrodysplasia punctata of Happle
Applies To
  • Albright (-McCune)-Sternberg syndrome
ICD-9-CM Volume 2 Index entries containing back-references to 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
    • 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
      • osseous 277.5
  • 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
  • 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
 756.56 ICD9Data.com 756.6 
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