Home > 2012 ICD-9-CM Diagnosis Codes > Congenital Anomalies 740-759 > Other congenital musculoskeletal anomalies 756-
2012 ICD-9-CM Diagnosis Code 756.9
Other and unspecified anomalies of musculoskeletal system
- Short description: Musculoskel anom NEC/NOS.
- ICD-9-CM 756.9 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
- You are viewing the 2012 version of ICD-9-CM 756.9.
- More recent version(s) of ICD-9-CM 756.9: 2013.
756.9 Alternative Terminology
- Aberrant forearm extensor muscle
- Aberrant forearm flexor muscle
- Aberrant intrinsic muscles of hand
- Aberrant muscle of the lower limb
- Aberrant muscle of the upper limb
- Abnormal endochondral bone formation
- Absence of bone in arm
- Absent bone in foot
- Absent bone in hand
- Absent patella
- Accessory ossification center
- Acephalogaster
- Achondrogenesis, type ia
- Acromesomelic dysplasia group
- Acroscyphodysplasia
- Atelosteogenesis type 2
- Atelosteogenesis/diastrophic dysplasia
- Autosomal recessive spondyloepimetaphyseal dysplasia
- Beals auriculo-osteodysplasia syndrome
- Bone absent
- Bone and joint malformation
- Bone island
- Boomerang dysplasia
- Brachydactyly syndrome type e
- Certain congenital musculoskeletal deformities
- Chondrodysplasia punctata group
- Combined malformation of central nervous system and skeletal muscle
- Congenital absence of skeletal bone
- Congenital anomaly of bone and joint
- Congenital anomaly of cartilage
- Congenital anomaly of hyoid bone
- Congenital anomaly of joint
- Congenital anomaly of musculoskeletal structure of trunk
- Congenital anomaly of musculoskeletal system
- Congenital anomaly of skeletal bone
- Congenital connective tissue disorder
- Congenital malformation of musculoskeletal system
- Congenital skeletal dysplasia
- Cranioectodermal dysplasia
- Defects of the tubular bones and/or axial skeleton
- Deposition in skeletal muscle
- Desbuquois syndrome
- Disorder of bone development
- Disorder: ectopic bone tissue, congenital
- Disorganized development of cartilaginous and fibrous components of the skeleton
- Dysmorphia
- Dysmorphism
- Dysmorphological structure
- Dysosteosclerosis
- Dysostosis
- Dysostosis multiplex
- Dysostosis multiplex group
- Dysplasia of epiphysis
- Dysplasia with decreased bone density
- Dysplasia with defective mineralization
- Dysplasia with increased bone density
- Dysplasia, epiphysis
- Dysplasia, metaphyseal
- Dysplasias with significant membranous bone involvement
- Endosteal hyperostoses
- Endosteal hyperostoses with cerebellar hypoplasia
- Epiphyseal dysplasia
- Familial expansile osteolysis
- Finding of arrangement of skeletal muscle
- Hereditary acrosteolysis
- Hypochondrogenesis
- Hypochondroplasia
- Idiopathic multicentric osteolysis
- Idiopathic osteolyses
- Incomplete ossification of arch of caudal vertebra
- Infantile myofibromatosis
- Jarcho-levin syndrome
- Kniest dysplasia
- Kniest-stickler dysplasia
- Leri's pleonosteosis syndrome
- Lordosis in skeletal dysplasia
- Mesomelic dysplasia
- Metaphyseal anadysplasia
- Metaphyseal dysplasia
- Mild spondyloepiphyseal dysplasia with premature onset arthrosis
- Multiple congenital articular rigidities
- Multiple dislocations with dysplasia
- Myopathy with abnormality of histochemical fiber type
- Myopathy with tubular aggregates
- Paralytic calcification / ossification of muscle
- Precocious osteodysplasty
- Progressive pseudorheumatoid dysplasia
- Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
- Pseudochondroplasia
- Pseudodiastrophic dysplasia
- Pyle metaphyseal dysplasia
- Raine dysplasia
- Schneckenbecken dysplasia
- Scypho-patellar dysplasia
- Sialic storage disease
- Sponastrime dysplasia
- Spondylodysplasia
- Spondylodysplasia, luton type
- Spondylodysplasia, san diego type
- Spondylodysplasia, torrance type
- Spondylodysplastic group
- Spondyloenchondrodysplasia
- Spondyloenchondromatosis with basal ganglia calcification
- Spondyloepihphyseal dysplasia tarda
- Spondyloepimetaphyseal disorder
- Spondyloepimetaphyseal dysplasia
- Spondyloepimetaphyseal dysplasia with joint laxity
- Spondyloepiphyseal dysplasia congenita
- Spondyloepiphyseal dysplasia congenita group
- Spondyloepiphyseal dysplasia congenitalita
- Spondyloepiphyseal dysplasia tarda
- Type iv short rib polydactyly syndrome
Applies To
- Congenital:
- anomaly NOS of musculoskeletal system, NEC
- deformity NOS of musculoskeletal system, NEC
Convert 756.9 to ICD-10-CM 
ICD-9-CM Volume 2 Index entries containing back-references to 756.9:
- Abnormal, abnormality, abnormalities - see also Anomaly
synchondrosis 756.9
- Absence (organ or part) (complete or partial)
bone (congenital) NEC 756.9
- cartilage 756.9
- musculoskeletal system (congenital) NEC 756.9
- Accessory (congenital)
- bone NEC 756.9
foot 755.67
- Agenesis - see also Absence, by site, congenital
- bone NEC 756.9
- cartilage 756.9
- musculoskeletal system NEC 756.9
- Anomaly, anomalous (congenital) (unspecified type) 759.9
- bone NEC 756.9
- bursa 756.9
- cartilaginous 756.9
- connective tissue 756.9
specified type NEC 756.89
- fascia 756.9
- specified type NEC 756.89
- musculoskeletal system, except limbs 756.9
- specified type NEC 756.9
- specified type NEC
- adrenal (gland) 759.1
- alimentary tract (complete) (partial) 751.8
- ankle 755.69
- anus, anal (canal) 751.5
- aorta, aortic 747.29
- arch 747.21
- appendix 751.5
- arm 755.59
- artery (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
- auditory canal 744.29
- causing impairment of hearing 744.02
- bile duct or passage 751.69
- bladder 753.8
- neck 753.8
- bone(s) 756.9
- brain 742.4
- breast 757.6
- broad ligament 752.19
- bronchus 748.3
- canal of Nuck 752.89
- cardiac septal closure 745.8
- carpus 755.59
- cartilaginous 756.9
- cecum 751.5
- cervix 752.49
- chest (wall) 756.3
- chin 744.89
- ciliary body 743.46
- circulatory system 747.89
- clavicle 755.51
- clitoris 752.49
- coccyx 756.19
- colon 751.5
- common duct 751.69
- connective tissue 756.89
- cricoid cartilage 748.3
- cystic duct 751.69
- diaphragm 756.6
- digestive organ(s) or tract 751.8
- duodenum 751.5
- ear 744.29
- ejaculatory duct 752.89
- endocrine 759.2
- epiglottis 748.3
- esophagus 750.4
- Eustachian tube 744.24
- eye 743.8
- face 744.89
- bone(s) 756.0
- fallopian tube 752.19
- fascia 756.89
- femur 755.69
- fibula 755.69
- finger 755.59
- foot 755.67
- fovea centralis 743.55
- gallbladder 751.69
- Gartner's duct 752.89
- gastrointestinal tract 751.8
- genitalia, genital organ(s)
- genitourinary tract NEC 752.89
- glottis 748.3
- hair 757.4
- hand 755.59
- heart 746.89
- hepatic duct 751.69
- hydatid of Morgagni 752.89
- hymen 752.49
- integument 757.8
- intestine (large) (small) 751.5
- fixational type 751.4
- iris 743.46
- jejunum 751.5
- joint 755.8
- kidney 753.3
- knee 755.64
- labium (majus) (minus) 752.49
- labyrinth, membranous 744.05
- larynx 748.3
- leg 755.69
- lens 743.39
- limb, except reduction deformity 755.8
- lip 750.26
- liver 751.69
- lung (fissure) (lobe) 748.69
- meatus urinarius 753.8
- metacarpus 755.59
- mouth 750.26
- Müllerian
- muscle 756.89
- eye 743.69
- musculoskeletal system, except limbs 756.9
- nail 757.5
- neck 744.89
- nerve 742.8
- nervous system 742.8
- nipple 757.6
- nose 748.1
- organ NEC 759.89
- of Corti 744.05
- osseous meatus (ear) 744.03
- ovary 752.0
- oviduct 752.19
- pancreas 751.7
- parathyroid 759.2
- patella 755.64
- pelvic girdle 755.69
- penis 752.69
- pericardium 746.89
- peripheral vascular system NEC (see also Anomaly, peripheral vascular system) 747.60
- pharynx 750.29
- pituitary 759.2
- prostate 752.89
- radius 755.59
- rectum 751.5
- respiratory system 748.8
- rib 756.3
- round ligament 752.89
- sacrum 756.19
- salivary duct or gland 750.26
- scapula 755.59
- sclera 743.47
- scrotum 752.89
- transposition 752.81
- seminal duct or tract 752.89
- shoulder girdle 755.59
- site NEC 759.89
- skin 757.39
- skull (bone(s)) 756.0
- specified organ or site NEC 759.89
- spermatic cord 752.89
- spinal cord 742.59
- spine 756.19
- spleen 759.0
- sternum 756.3
- stomach 750.7
- tarsus 755.67
- tendon 756.89
- testis 752.89
- thorax (wall) 756.3
- thymus 759.2
- thyroid (gland) 759.2
- cartilage 748.3
- tibia 755.69
- toe 755.66
- tongue 750.19
- trachea (cartilage) 748.3
- ulna 755.59
- urachus 753.7
- ureter 753.4
- obstructive 753.29
- urethra 753.8
- obstructive 753.6
- urinary tract 753.8
- uterus (Müllerian) 752.39
- uvula 750.26
- vagina 752.49
- vascular NEC (see also Anomaly, peripheral vascular system) 747.60
- brain 747.81
- vas deferens 752.89
- vein(s) (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
- vena cava (inferior) (superior) 747.49
- vertebra 756.19
- vulva 752.49
- tendon 756.9
- specified type NEC 756.89
- Deformity 738.9
- bursa, congenital 756.9
- ligament (acquired) 728.9
- congenital 756.9
- muscle (acquired) 728.9
- musculoskeletal system, congenital NEC 756.9
- specified type NEC 756.9
- Development
- abnormal, bone 756.9
- Dysplasia - see also Anomaly
- epiphysis 756.9
- multiple 756.56
- metaphyseal 756.9
- familial 756.89
- Elongation, elongated (congenital) - see also Distortion
- bone 756.9
- Fracture (abduction) (adduction) (avulsion) (compression) (crush) (dislocation) (oblique) (separation) (closed) 829.0
- congenital 756.9
- Fusion, fused (congenital)
- bone 756.9
- ossicles 756.9
- auditory 744.04
- Hypoplasia, hypoplasis 759.89
- bone NEC 756.9
- cartilaginous 756.9
- Malformation (congenital) - see also Anomaly
- bone 756.9
- bursa 756.9
- muscle 756.9
- tendon 756.9
- Rudimentary (congenital) - see also Agenesis
- bone 756.9
- Segmentation, incomplete (congenital) - see also Fusion
- bone NEC 756.9
- Supernumerary (congenital)
- bone 756.9
- Synchondrosis 756.9
- abnormal (congenital) 756.9
- ischiopubic (van Neck's) 732.1
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 756.9 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 2012 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
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