756.59 OSTEODYSTROPHY NEC


Code Information

Diagnosis Code: 756.59

Short Description: Osteodystrophy NEC

Long Description: Other osteodystrophies

Code Classification:

  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 756 Other congenital musculoskeletal anomalies
        • 756.59 Osteodystrophy NEC

Code Version: 2015 ICD-9-CM


Synonyms

  • Acrodysostosis
  • Acromicric dysplasia
  • Bent bone dysplasia
  • Capitate-hamate synostosis
  • Carpal-tarsal osteolysis with nephropathy
  • Chondrodysplasia punctata congenita
  • Chondrodysplasia punctata, Conradi-Hünermann type
  • Chondrodysplasia punctata, tibia-metacarpal 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
  • Dolichospondylic dysplasia
  • 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
  • Progressive diaphyseal dysplasia
  • Rolland-Debuqois syndrome
  • Sclerosteosis
  • Spondyloepiphyseal dysplasia congenita
  • Ulnar and humeroulnar synostosis
  • X-linked dominant chondrodysplasia punctata of Happle

References to Index of Diseases and Injuries

The code 756.59 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • 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 (-H�nermann) 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 (-H�nermann) 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
  • L�ri-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 (-H�nermann) (chondrodysplasia calcificans congenita) 756.59
    • Fuller Albright's (osteitis fibrosa disseminata) 756.59
    • L�ri-Weill 756.59
    • McCune-Albright (osteitis fibrosa disseminata) 756.59
    • Ostrum-Furst 756.59
  • Synostosis (congenital) 756.59
    • astragaloscaphoid 755.67
    • radioulnar 755.53
    • talonavicular (bar) 755.67
    • tarsal 755.67

Crosswalk Information

The code 756.59 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
756.59 Right Arrow Q78.8 Other specified osteochondrodysplasias
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
756.0 Anomalies of skull and face bones
756.10 Anomaly of spine, unspecified
756.11 Spondylolysis, lumbosacral region
756.12 Spondylolisthesis
756.13 Absence of vertebra, congenital
756.14 Hemivertebra
756.15 Fusion of spine (vertebra), congenital
756.16 Klippel-Feil syndrome
756.17 Spina bifida occulta
756.19 Other anomalies of spine
756.2 Cervical rib
756.3 Other anomalies of ribs and sternum
756.4 Chondrodystrophy
756.50 Congenital osteodystrophy, unspecified
756.51 Osteogenesis imperfecta
756.52 Osteopetrosis
756.53 Osteopoikilosis
756.54 Polyostotic fibrous dysplasia of bone
756.55 Chondroectodermal dysplasia
756.56 Multiple epiphyseal dysplasia
756.6 Anomalies of diaphragm
756.70 Anomaly of abdominal wall, unspecified
756.71 Prune belly syndrome
756.72 Omphalocele
756.73 Gastroschisis
756.79 Other congenital anomalies of abdominal wall
756.81 Absence of muscle and tendon
756.82 Accessory muscle
756.83 Ehlers-Danlos syndrome
756.89 Other specified anomalies of muscle, tendon, fascia, and connective tissue
756.9 Other and unspecified anomalies of musculoskeletal system


This page was last updated on: 10/1/2014