2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Congential Anomalies 740-759 > Other And Unspecified Congenital Anomalies 759.* > 2008 ICD-9-CM Diagnosis 759.82 Marfan syndrome  On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date. The 2009 version of ICD-9-CM 759.82 can be accessed here. A hereditary disorder of connective tissue characterized by tall stature, elongated extremities, subluxation of the lens, dilatation of the ascending aorta, and "pigeon breast." It is inherited as an autosomal dominant trait. 759.82 is a specific code that can be used to specify a diagnosis 759.82 contains 10 index entries View the ICD-9-CM Volume 1 759.* hierarchy ICD9Data's sister site ProcedureCodes.com launches with the 2008/09 CPT® codes - read more on the ICD9Data.com blog. Index entries containing 759.82: Acrochondrohyperplasia 759.82 Arachnodactyly 759.82 Beals syndrome 759.82 Disease, diseased - see also Syndrome Marfan's 090.49 meaning Marfan's syndrome 759.82 Dolichostenomelia 759.82 Dysmorodystrophia mesodermalis congenita 759.82 Dystrophy, dystrophia 783.9 mesodermalis congenita 759.82 Marfan's syndrome (arachnodactyly) 759.82 meaning congenital syphilis 090.49 with luxation of lens 090.49 [379.32] Syndrome - see also Disease Beals 759.82 Marfan's (arachnodactyly) 759.82 meaning congenital syphilis 090.49 with luxation of lens 090.49 [379.32]