Home > 2013 ICD-9-CM Diagnosis Codes > Congenital Anomalies 740-759 > Other congenital musculoskeletal anomalies 756-
2013 ICD-9-CM Diagnosis Code 756.59
Other osteodystrophies
- ICD-9-CM 756.59 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
756.59 Alternative Terminology
- 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
- 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
Convert 756.59 to ICD-10-CM 

ICD-9-CM 756.59 converts approximately to:
- 2013 ICD-10-CM Q78.8 Other specified osteochondrodysplasias
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
bone (fibrous) NEC 733.29
diaphyseal, progressive 756.59
fibrous
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
astragaloscaphoid 755.67
radioulnar 755.53
talonavicular (bar) 755.67
tarsal 755.67
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 756.59 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2013 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
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