Home > 2012 ICD-9-CM Diagnosis Codes > Congenital Anomalies 740-759 > Other congenital musculoskeletal anomalies 756-
2012 ICD-9-CM Diagnosis Code 756.89
Other specified anomalies of muscle, tendon, fascia, and connective tissue
- Short description: Soft tissue anomaly NEC.
- ICD-9-CM 756.89 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 756.89.
- More recent version(s) of ICD-9-CM 756.89: 2013.
756.89 Alternative Terminology
- Amyoplasia congenita disruptive sequence
- Amyoplasia, disruptive sequence
- Amyotrophia congenita
- Ayala's disease
- Congenital anomaly of muscle and/or tendon
- Congenital anomaly of skeletal muscle
- Congenital articular rigidity with myopathy
- Congenital contracture of gastrocnemius
- Congenital contracture of gastrocnemius muscle
- Congenital short quadriceps
- Congenital shortening of tendon
- Congenital trigger finger and trigger thumb
- Congenital trigger thumb
- Contracture of gastrocnemius, congenital
- Craniometadiaphyseal dysplasia
- Craniometaphyseal dysplasia
- Craniometaphyseal dysplasia - mild type
- Craniometaphyseal dysplasia - severe type
- Diastrophic dysplasia
- Failure of soft tissue differentiation of lower limb
- Hereditary osteoonychodysplasia
- Hypoplasia of muscle
- Melorheostosis
- Microcephalic osteodysplastic dysplasia
- Nail patella-like renal disease
- Nail-patella syndrome
- Nail-patella syndrome, hereditary osteoonychodysplasia
- Poland anomaly
- Popliteal pterygium syndrome
- Post-inflammatory cutis laxa
- Schwartz jampel syndrome
- Schwartz-jampel syndrome
- Waardenburg syndrome
- Waardenburg's syndrome
- Yunis-varon dysplasia
Applies To
- Amyotrophia congenita
- Congenital shortening of tendon
Convert 756.89 to ICD-10-CM 
ICD-9-CM 756.89 converts approximately to:
- 2013 ICD-10-CM Q79.8 Other congenital malformations of musculoskeletal system
ICD-9-CM Volume 2 Index entries containing back-references to 756.89:
- Accessory (congenital)
tendon 756.89
- Amyoplasia, congenita 756.89
- Amyotrophia, amyotrophy, amyotrophic 728.2
- congenita 756.89
- Anomaly, anomalous (congenital) (unspecified type) 759.9
connective tissue 756.9
specified type NEC 756.89
- fascia 756.9
- specified type NEC 756.89
- 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
- Arthro-onychodysplasia 756.89
- Arthro-osteo-onychodysplasia 756.89
- Ayala's disease 756.89
- Bakwin-Krida syndrome (craniometaphyseal dysplasia) 756.89
- Contraction, contracture, contracted
- ligament 728.89
- congenital 756.89
- muscle (postinfectional) (postural) NEC 728.85
- congenital 756.89
- sternocleidomastoid 754.1
- extraocular 378.60
- eye (extrinsic) (see also Strabismus) 378.9
- paralytic (see also Strabismus, paralytic) 378.50
- flaccid 728.85
- hysterical 300.11
- ischemic (Volkmann's) 958.6
- paralytic 728.85
- posttraumatic 958.6
- psychogenic 306.0
- specified as conversion reaction 300.11
- Deficiency, deficient
- Deformity 738.9
- Diastasis
- muscle 728.84
- congenital 756.89
- Disease, diseased - see also Syndrome
- Ayala's 756.89
- Pyle (-Cohn) (craniometaphyseal dysplasia) 756.89
- Dysplasia - see also Anomaly
- craniometaphyseal 756.89
- familial metaphyseal 756.89
- metaphyseal 756.9
- familial 756.89
- muscle 756.89
- osteo-onycho-arthro (hereditary) 756.89
- Elongation, elongated (congenital) - see also Distortion
- ligamentum patellae 756.89
- Fong's syndrome (hereditary osteoonychodysplasia) 756.89
- HOOD (hereditary osteo-onychodysplasia) 756.89
- Horn
- iliac 756.89
- Hypoplasia, hypoplasis 759.89
- muscle 756.89
- eye 743.69
- Krabbe's
- syndrome
- congenital muscle hypoplasia 756.89
- cutaneocerebral angioma 759.6
- Léris pleonosteosis 756.89
- Myelo-osteo-musculodysplasia hereditaria 756.89
- Nail - see also condition
- patella syndrome (hereditary osteoonychodysplasia) 756.89
- Onycho-osteodysplasia 756.89
- Osteo-onycho-arthro dysplasia 756.89
- Osteo-onychodysplasia, hereditary 756.89
- Österreicher-Turner syndrome 756.89
- Pyle (-Cohn) disease (craniometaphyseal dysplasia) 756.89
- Short, shortening, shortness
- Syndrome - see also Disease
- Bakwin-Krida (craniometaphyseal dysplasia) 756.89
- Fong's (hereditary osteo-onychodysplasia) 756.89
- Krabbe's
- congenital muscle hypoplasia 756.89
- cutaneocerebral angioma 759.6
- nail-patella (hereditary osteo-onychodysplasia) 756.89
- Österreicher-Turner (hereditary osteo-onychodysplasia) 756.89
- popliteal
- artery entrapment 447.8
- web 756.89
- Touraine's (hereditary osteo-onychodysplasia) 756.89
- Touraine's syndrome (hereditary osteo-onychodysplasia) 756.89
- Trigger finger (acquired) 727.03
- congenital 756.89
- Turner-Kieser syndrome (hereditary osteo-onychodysplasia) 756.89
- Waardenburg's syndrome 756.89
- meaning ptosis-epicanthus 270.2
- Web, webbed (congenital) - see also Anomaly, specified type NEC
- popliteal syndrome 756.89
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 756.89 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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