Diagnosis Code: 756.89

Short Description: Soft tissue anomaly NEC

Long Description: Other specified anomalies of muscle, tendon, fascia, and connective tissue

Code Classification:

• Congenital anomalies (740–759)
  • Congenital anomalies (740-759)
    • 756 Other congenital musculoskeletal anomalies
      • 756.89 Soft tissue anomaly NEC

Code Version: 2015 ICD-9-CM

Synonyms

• Amyoplasia congenita 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 muscle
• Congenital short quadriceps
• Congenital shortening of tendon
• Congenital trigger thumb
• Craniometadiaphyseal dysplasia
• Craniometaphyseal dysplasia
• Craniometaphyseal dysplasia - mild type
• Craniometaphyseal dysplasia - severe type
• Diastrophic dysplasia
• Failure of soft tissue differentiation of lower limb
• Hypoplasia of muscle
• Melorheostosis
• Microcephalic osteodysplastic dysplasia
• Myostatin related hypertrophy of muscle
• Nail patella-like renal disease
• Poland anomaly
• Popliteal pterygium syndrome
• Post-inflammatory cutis laxa
• Waardenburg's syndrome
• Yunis-Varon dysplasia

References to Index of Diseases and Injuries

The code 756.89 has the following ICD-9-CM references to the Index of Diseases and Injuries

• 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

• L�ris 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

• �sterreicher-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
  • �sterreicher-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

Crosswalk Information

The code 756.89 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

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