2008 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 Mineral Metabolism 275.* >  2008 ICD-9-CM Diagnosis 275.0
Disorders of iron metabolism 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 Therefore, this code may be out of date.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 275.0 can be accessed here. - A disorder due to the deposition of hemosiderin in the parenchymal cells, causing tissue damage and dysfunction of the liver, pancreas, heart, and pituitary. Full development of the disease in women is restricted by menstruation, pregnancy, and lower dietary intake of iron. Acquired hemochromatosis may be the result of blood transfusions, excessive dietary iron, or secondary to other disease. Idiopathic or genetic hemochromatosis is an autosomal recessive disorder of metabolism associated with a gene tightly linked to the A locus of the HLA complex on chromosome 6. (From Dorland, 27th ed)
- Disorders in the processing of iron in the body: its absorption, transport, storage, and utilization. (From Mosby's Medical, Nursing, & Allied Health Dictionary, 4th ed)
- 275.0 is a specific code that can be used to specify a diagnosis
- 275.0 contains 30 index entries
- View the ICD-9-CM Volume 1 275.* hierarchy
275.0 also known as:- Bronzed diabetes
- Hemochromatosis
- Pigmentary cirrhosis (of liver)
275.0 excludes:
Index entries containing 275.0:- Bronze, bronzed
- diabetes
 275.0
Cirrhosis, cirrhotic 571.5- due to
- bronzed diabetes 275.0
- hemochromatosis 275.0
- liver (chronic) (hepatolienal) (hypertrophic) (nodular) (splenomegalic) (unilobar) 571.5
- pigmentary 275.0
- pigment, pigmentary (of liver) 275.0
Diabetes, diabetic (brittle) (congenital) (familial) (mellitus) (poorly controlled) (severe) (slight) (without complication) 250.0- bronze, bronzed 275.0
- hemochromatosis 275.0
Disease, diseased - see also Syndrome- iron
- metabolism 275.0
- storage 275.0
- Recklinghausen-Applebaum (hemochromatosis) 275.0
- von Recklinghausen-Applebaum (hemochromatosis) 275.0
Disorder - see also Disease- iron, metabolism 275.0
- metabolism NEC 277.9
- hemochromatosis 275.0
- iron 275.0
- storage, iron 275.0
Disturbance - see also Disease- metabolism (acquired) (congenital) (see also Disorder, metabolism) 277.9
- general 277.9
- iron 275.0
- iron 275.0
Hanot-Chauffard (-Troisier) syndrome (bronze diabetes) 275.0
Hemochromatosis (acquired) (diabetic) (hereditary) (liver) (myocardium) (primary idiopathic) (secondary) 275.0Hemosiderosis 275.0- dietary 275.0
- pulmonary (idiopathic) 275.0 [516.1]
- transfusion NEC 999.8
Infiltrate, infiltration- with an iron compound 275.0
Iron- metabolism disease 275.0
- storage disease 275.0
Melanemia 275.0
Recklinghausen-Applebaum disease (hemochromatosis) 275.0
Syndrome - see also Disease- Hanot-Chauffard (-Troisier) (bronze diabetes) 275.0
- Troisier-Hanot-Chauffard (bronze diabetes) 275.0
Troisier-Hanot-Chauffard syndrome (bronze diabetes) 275.0
von Recklinghausen-Applebaum disease (hemochromatosis) 275.0
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