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 Therefore, this code may be out of date.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
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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
Syndrome - see also Disease- Beals
759.82
- Marfan's (arachnodactyly)
759.82- meaning congenital syphilis 090.49
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