2008 ICD-9-CM Diagnosis Code 756.9 : Other and unspecified congenital anomalies of musculoskeletal system

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2008 ICD-9-CM Diagnosis Code 756.9

Other and unspecified congenital 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 indicate a diagnosis on a reimbursement claim, however, 756.9 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
You are viewing the 2008 version of ICD-9-CM 756.9.
More recent version(s) of ICD-9-CM 756.9: 2009 2010 2011 2012 2013 2014 2015.

Convert to ICD-10-CM: 756.9 converts approximately to:

2015/16 ICD-10-CM Q68.8 Other specified congenital musculoskeletal deformities
Or:
2015/16 ICD-10-CM Q79.8 Other congenital malformations of musculoskeletal system
Or:
2015/16 ICD-10-CM Q79.9 Congenital malformation of musculoskeletal system, unspecified

Approximate Synonyms

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

ICD-9-CM Volume 2 Index entries containing back-references to 756.9:

Abnormal, abnormality, abnormalities - see also Anomaly
- development, developmental NEC 759.9
  - bone 756.9
  - central nervous system 742.9
- synchondrosis 756.9
Absence (organ or part) (complete or partial)
- bone (congenital) NEC 756.9
  - marrow 284.9
    - acquired (secondary) 284.89
    - congenital 284.09
    - hereditary 284.09
    - idiopathic 284.9
  - skull 756.0
- 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
  - ankle 755.69
  - arm 755.50
  - chest 756.3
  - cranium 756.0
  - face 756.0
  - finger 755.50
  - foot 755.67
  - forearm 755.50
  - frontal 756.0
  - head 756.0
  - hip 755.63
  - leg 755.60
  - lumbosacral 756.10
  - nose 748.1
  - pelvic girdle 755.60
  - rachitic 756.4
  - rib 756.3
  - shoulder girdle 755.50
  - skull 756.0
    - with
      - anencephalus 740.0
      - encephalocele 742.0
      - hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
      - microcephalus 742.1
  - toe 755.66
- bursa 756.9
- cartilaginous 756.9
- connective tissue 756.9
  - specified type NEC 756.89
- fascia 756.9
  - specified type NEC 756.89
- ligament 756.9
  - broad 752.10
  - round 752.9
- muscle 756.9
  - eye 743.9
    - specified type NEC 743.69
  - 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
    - lower 751.5
    - upper 750.8
  - 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
    - brain 747.81
    - coronary 746.85
    - eye 743.58
    - pulmonary 747.3
    - retinal 743.58
    - umbilical 747.5
  - 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
    - arm 755.59
    - face 756.0
    - leg 755.69
    - pelvic girdle 755.69
    - shoulder girdle 755.59
    - skull 756.0
      - with
        anencephalus 740.0
        encephalocele 742.0
        hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
        microcephalus 742.1
  - 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
    - lower 751.5
    - upper 750.8
  - duodenum 751.5
  - ear 744.29
    - auricle 744.29
      - causing impairment of hearing 744.02
    - causing impairment of hearing 744.09
    - inner (causing impairment of hearing) 744.05
    - middle, except ossicles 744.03
      - ossicles 744.04
  - ejaculatory duct 752.89
  - endocrine 759.2
  - epiglottis 748.3
  - esophagus 750.4
  - Eustachian tube 744.24
  - eye 743.8
    - lid 743.63
    - muscle 743.69
  - 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)
    - female 752.89
      - external 752.49
      - internal NEC 752.89
    - male 752.89
      - penis 752.69
      - scrotal transposition 752.81
  - genitourinary tract NEC 752.89
  - glottis 748.3
  - hair 757.4
  - hand 755.59
  - heart 746.89
    - valve NEC 746.89
      - pulmonary 746.09
  - 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
    - lower 755.69
      - reduction deformity (see also Deformity, reduction, lower limb) 755.30
    - upper 755.59
      - reduction deformity (see also Deformity, reduction, upper limb) 755.20
  - lip 750.26
  - liver 751.69
  - lung (fissure) (lobe) 748.69
  - meatus urinarius 753.8
  - metacarpus 755.59
  - mouth 750.26
  - muscle 756.89
    - eye 743.69
  - musculoskeletal system, except limbs 756.9
  - nail 757.5
  - neck 744.89
  - nerve 742.8
    - acoustic 742.8
    - optic 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
    - with
      - anencephalus 740.0
      - encephalocele 742.0
      - hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
      - microcephalus 742.1
  - 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 752.3
  - 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
    - brain 747.81
    - great 747.49
    - portal 747.49
    - pulmonary 747.49
  - vena cava (inferior) (superior) 747.49
  - vertebra 756.19
  - vulva 752.49
- tendon 756.9
  - specified type NEC 756.89
Deformity 738.9
- bone (acquired) NEC 738.9
  - congenital 756.9
  - turbinate 738.0
- bursa, congenital 756.9
- ligament (acquired) 728.9
  - congenital 756.9
- muscle (acquired) 728.9
  - congenital 756.9
    - specified type NEC 756.89
    - sternocleidomastoid (due to intrauterine malposition and pressure) 754.1
- musculoskeletal system, congenital NEC 756.9
  - specified type NEC 756.9
Development
- abnormal, bone 756.9
Dysplasia - see also Anomaly
- epiphysealis 756.9
  - multiplex 756.56
  - punctata 756.59
- 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
  - face 756.0
  - malar 756.0
  - mandible 524.04
    - alveolar 524.74
  - marrow 284.9
    - acquired (secondary) 284.89
    - congenital 284.09
    - idiopathic 284.9
  - maxilla 524.03
    - alveolar 524.73
  - skull (see also Hypoplasia, skull) 756.0
- 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

756.89

ICD9Data.com

757

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 2008 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.

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