
2009 ICD-9-CM Diagnosis Code 756.89
Other specified congenital 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 indicate a diagnosis on a reimbursement claim, however, 756.89 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 2009 version of ICD-9-CM 756.89.
- More recent version(s) of ICD-9-CM 756.89: 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM:
756.89 converts approximately to:
- 2015/16 ICD-10-CM Q79.8 Other congenital malformations of musculoskeletal system
Approximate Synonyms
- 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 bilat gastrocnemius
- Congenital contracture of bilateral gastrocnemius
- Congenital contracture of gastrocnemius
- Congenital contracture of gastrocnemius muscle
- Congenital contracture of left gastrocnemius
- Congenital contracture of right gastrocnemius
- 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
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

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

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


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

ejaculatory duct 752.89

endocrine 759.2

epiglottis 748.3

esophagus 750.4

Eustachian tube 744.24

eye 743.8

face 744.89

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

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
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

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

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

tibia 755.69

toe 755.66

tongue 750.19

trachea (cartilage) 748.3

ulna 755.59

urachus 753.7

ureter 753.4

urethra 753.8

urinary tract 753.8

uterus 752.3

uvula 750.26

vagina 752.49

vascular NEC (see also Anomaly, peripheral vascular system) 747.60

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
- Deficiency, deficient
short stature homeobox gene (SHOX)
with

dyschondrosteosis 756.89

short stature (idiopathic) 783.43


Turner's syndrome 758.6
- Deformity 738.9

muscle (acquired) 728.9

congenital 756.9


specified type NEC 756.89

sternocleidomastoid (due to intrauterine malposition and pressure) 754.1
- 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
- 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