2010 ICD-9-CM Diagnosis Code 756.89 : Other specified congenital anomalies of muscle tendon fascia and connective tissue

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2010 ICD-9-CM Diagnosis Code 756.89

Other specified congenital anomalies of muscle tendon fascia and connective tissue

756.83

756.9

756.89 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.

Also applicable to/known as Click to expand

ICD-9-CM Volume 2 Index Entries That Refer To 756.89 Click to expand

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
muscle 756.9
- specified type NEC 756.89
specified type NEC
- connective tissue 756.89
- fascia 756.89
- muscle 756.89
  - eye 743.69
- tendon 756.89
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

Deficiency, deficient

short stature homeobox gene (SHOX)
- with
  - dyschondrosteosis 756.89

Deformity 738.9

muscle (acquired) 728.9
- congenital 756.9
  - specified type NEC 756.89

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

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

tendon 727.81
- congenital 756.89

Syndrome - see also Disease

Bakwin-Krida (craniometaphyseal dysplasia) 756.89
Fong's (hereditary osteo-onychodysplasia) 756.89
Krabbe's
- congenital muscle hypoplasia 756.89
nail-patella (hereditary osteo-onychodysplasia) 756.89
Österreicher-Turner (hereditary osteo-onychodysplasia) 756.89
popliteal
- 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

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