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Free ICD-9-CM Diagnosis Codes > 2008 > Congential Anomalies 740-759 > Other congenital musculoskeletal anomalies 756.* >
Red triangle imageICD-9-CM Diagnosis 756
Other congenital musculoskeletal anomalies
Green triangle imageICD-9-CM Diagnosis 756.0
Congenital anomalies of skull and face bones
  • autosomal dominant disorder characterized by acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, and hypoplastic maxilla with relative mandibular prognathism.
  • premature closure of one or more sutures of the skull.
Red triangle imageICD-9-CM Diagnosis 756.1
Congenital anomalies of spine
Green triangle imageICD-9-CM Diagnosis 756.10
Congenital anomaly of spine unspecified
Green triangle imageICD-9-CM Diagnosis 756.11
Congenital spondylolysis lumbosacral region
Green triangle imageICD-9-CM Diagnosis 756.12
Spondylolisthesis congenital
Green triangle imageICD-9-CM Diagnosis 756.13
Absence of vertebra congenital
Green triangle imageICD-9-CM Diagnosis 756.14
Hemivertebra
Green triangle imageICD-9-CM Diagnosis 756.15
Fusion of spine (vertebra) congenital
Green triangle imageICD-9-CM Diagnosis 756.16
Klippel-feil syndrome
Green triangle imageICD-9-CM Diagnosis 756.17
Spina bifida occulta
Green triangle imageICD-9-CM Diagnosis 756.19
Other congenital anomalies of spine
Green triangle imageICD-9-CM Diagnosis 756.2
Cervical rib
Green triangle imageICD-9-CM Diagnosis 756.3
Other congenital anomalies of ribs and sternum
Green triangle imageICD-9-CM Diagnosis 756.4
Chondrodystrophy
  • autosomal dominant disorder that is the most frequent form of short-limb dwarfism; a disturbance of epiphyseal chondroblastic growth, causing inadequate enchondral bone formation.
  • 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. (MeSH)
  • morbid condition characterized by abnormal development of cartilage.
  • A rare benign disorder characterized by lack of normal endchondral ossification, and the growth of multiple enchondromas. It primarily affects the bones of the hand, in children and young adults. Extent of the disease varies; in some cases, neoplastic involvement may be wide spread causing considerable deformity.
Red triangle imageICD-9-CM Diagnosis 756.5
Congenital osteodystrophies
Green triangle imageICD-9-CM Diagnosis 756.50
Congenital osteodystrophy unspecified
Green triangle imageICD-9-CM Diagnosis 756.51
Osteogenesis imperfecta
  • autosomal dominant collagen disease resulting from defective biosynthesis of collagen type I and characterized by brittle, osteoporotic, and easily fractured bones; may also present with blue sclerae, loose joints, and imperfect dentin formation.
Green triangle imageICD-9-CM Diagnosis 756.52
Osteopetrosis
  • excessive formation of dense trabecular bone leading to pathological fractures, osteitis, splenomegaly with infarct, anemia, and extramedullary hemopoiesis.
Green triangle imageICD-9-CM Diagnosis 756.53
Osteopoikilosis
Green triangle imageICD-9-CM Diagnosis 756.54
Polyostotic fibrous dysplasia of bone
Green triangle imageICD-9-CM Diagnosis 756.55
Chondroectodermal dysplasia
  • Chondrodysplasia of long bones affecting mainly the distal ends of extremities and resulting in short-limb dwarfism, hexadactyly of the fingers and less frequently the toes; ectodermal dysplasia with nail and hair abnormalities, and congenital heart defects. Associated abnormalities may include cryptorchidism, epispadias, talipes equinovalgus, and Dandy-Walker syndrome (absence of cerebellar vermis, hydrocephalus, and posterior fossa cyst continuous with the fourth ventricle). Some patients are retarded. The largest pedigree was observed in Old Order Amish in Lancaster County, Pennsylvania and some cases were reported in Australian Aborigines.
Green triangle imageICD-9-CM Diagnosis 756.56
Multiple epiphyseal dysplasia
Green triangle imageICD-9-CM Diagnosis 756.59
Other congenital osteodystrophies
Green triangle imageICD-9-CM Diagnosis 756.6
Congenital anomalies of diaphragm
Red triangle imageICD-9-CM Diagnosis 756.7
Congenital anomalies of abdominal wall
Green triangle imageICD-9-CM Diagnosis 756.70
Anomaly of abdominal wall unspecified
Green triangle imageICD-9-CM Diagnosis 756.71
Prune belly syndrome
  • A syndrome of hypoplasia or aplasia of the abdominal muscle, presenting a thin, loose, wrinkled and shriveled (prunelike) abdominal wall, with furrowlike umbilicus, and other anomalies, including persistent urachus, pigeon breast deformity, and a variety of gastrointestinal, cardiovascular, urogenital, and skeletal abnormalities. Prune belly syndrome may occur with or without pulmonic stenosis, deafness, and mental retardation. Distention of the bladder and urethra in utero is considered as a possible cause of abdominal overdistention.
Green triangle imageICD-9-CM Diagnosis 756.79
Other congenital anomalies of abdominal wall
Red triangle imageICD-9-CM Diagnosis 756.8
Other specified congenital anomalies of muscle tendon fascia and connective tissue
Green triangle imageICD-9-CM Diagnosis 756.81
Congenital absence of muscle and tendon
Green triangle imageICD-9-CM Diagnosis 756.82
Accessory muscle
Green triangle imageICD-9-CM Diagnosis 756.83
Ehlers-danlos syndrome
  • group of inherited disorders of the connective tissue; major manifestations include hyperextensible skin and joints, easy bruisability, friability of tissues with bleeding and poor wound healing, calcified subcutaneous spheroids, and pseudotumors.
Green triangle imageICD-9-CM Diagnosis 756.89
Other specified congenital anomalies of muscle tendon fascia and connective tissue
Green triangle imageICD-9-CM Diagnosis 756.9
Other and unspecified congenital anomalies of musculoskeletal system
Other congenital anomalies of limbs 755.*
  
757.* Congenital anomalies of the integument