2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders 240-279 > Other Metabolic Disorders And Immunity Disorders 270-279 > Disorders Of Carbohydrate Transport And Metabolism 271.* >
 2007 ICD-9-CM Diagnosis 271.1
Galactosemia 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 Therefore, this code may be out of date.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 271.1 can be accessed here. - A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (OVARIAN FAILURE, PREMATURE); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)
- 271.1 is a specific code that can be used to specify a diagnosis
- 271.1 contains 6 index entries
- View the ICD-9-CM Volume 1 271.* hierarchy
271.1 also known as:- Galactose-1-phosphate uridyl transferase deficiency
- Galactosuria
Index entries containing 271.1:- Deficiency, deficient
- galactokinase
 271.1
- galactose-1-phosphate uridyl transferase 271.1
Disorder - see also Disease- metabolism NEC 277.9
- galactose-1-phosphate uridyl transferase 271.1
Galactosemia (classic) (congenital) 271.1
Galactosuria 271.1
Malabsorption 579.9- galactose 271.1
|
|
|
