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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 756.4

Chondrodystrophy

This code may be outdated. View the most recent version of ICD-9-CM 756.4

  • An autosomal dominant disorder that is the most frequent form of short-limb dwarfism. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and mid-face hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, genu varum, and trident hand. (Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim, MIM#100800, April 20, 2001)
  • Benign growths of cartilage in the metaphyses of several bones.
  • 756.4 is a specific code that can be used to specify a diagnosis
  • 756.4 contains 40 index entries
  • View the ICD-9-CM Volume 1 756.* hierarchy

756.4 also known as:

  • Achondroplasia
  • Chondrodystrophia (fetalis)
  • Dyschondroplasia
  • Enchondromatosis
  • Ollier's disease

756.4 excludes:

  • lipochondrodystrophy [Hurler's syndrome] (277.5)
  • Morquio's disease (277.5)

Index entries containing 756.4:

Achondroplasia 756.4
Aclasis
  • diaphyseal 756.4
Anomaly, anomalous (congenital) (unspecified type) 759.9
  • bone NEC 756.9
    • rachitic 756.4
  • pelvis (bony) 755.60
    • rachitic 268.1
      • fetal 756.4
  • rachitic, fetal 756.4
Chondrodysplasia 756.4
  • angiomatose 756.4
  • calcificans congenita 756.59
  • epiphysialis punctata 756.59
  • hereditary deforming 756.4
  • rhizomelic punctata 277.86
Chondrodystrophia (fetalis) 756.4Chondrodystrophy (familial) (hypoplastic) 756.4
Diaphyseal aclasis 756.4
Disease, diseased - see also Syndrome
  • Jeune's (asphyxiating thoracic dystrophy) 756.4
  • Ollier's (chondrodysplasia) 756.4
  • Voorhoeve's (dyschondroplasia) 756.4
Dwarf, dwarfism 259.4
  • achondroplastic 756.4
  • metatropic 756.4
Dyschondroplasia (with hemangiomata) 756.4
  • Voorhoeve's 756.4
Dysplasia - see also Anomaly
  • chondromatose 756.4
Dystrophy, dystrophia 783.9
  • asphyxiating thoracic 756.4
  • thoracic asphyxiating 756.4
Enchondroma (M9220/0) - see also Neoplasm, bone, benign
  • multiple, congenital 756.4
Enchondromatosis (cartilaginous) (congenital) (multiple) 756.4
Enchondroses, multiple (cartilaginous) (congenital) 756.4
Exostosis 726.91
  • congenital 756.4
  • multiple (cancellous) (congenital) (hereditary) 756.4
Jeune's disease or syndrome (asphyxiating thoracic dystrophy) 756.4
Kast's syndrome (dyschondroplasia with hemangiomas) 756.4
Maffucci's syndrome (dyschondroplasia with hemangiomas) 756.4
Ollier's disease (chondrodysplasia) 756.4
Osteochondrodystrophy 277.5
  • fetalis 756.4
Osteochondroma (M9210/0) - see also Neoplasm, bone, benign
  • multiple, congenital 756.4
Osteopathia
  • striata 756.4
Rachitis, rachitism - see also Rickets
  • fetalis 756.4
Rickets (active) (acute) (adolescent) (adult) (chest wall) (congenital) (current) (infantile) (intestinal) 268.0
  • fetal 756.4
Syndrome - see also Disease
  • Jeune's (asphyxiating thoracic dystrophy of newborn) 756.4
  • Kast's (dyschondroplasia with hemangiomas) 756.4
  • Maffucci's (dyschondroplasia with hemangiomas) 756.4
Voorhoeve's disease or dyschondroplasia 756.4