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2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Other Congenital Musculoskeletal Anomalies 756.* > 2007 ICD-9-CM Diagnosis 756.89 Other specified congenital anomalies of muscle tendon fascia and connective tissue This code may be outdated. View the most recent version of ICD-9-CM 756.89 756.89 is a specific code that can be used to specify a diagnosis 756.89 contains 55 index entries View the ICD-9-CM Volume 1 756.* hierarchy 756.89 also known as: Amyotrophia congenita Congenital shortening of tendon Index entries containing 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 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 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 Schwartz (-Jampel) syndrome 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 Schwartz (-Jampel) 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