2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > Other Diseases Of Blood And Blood-Forming Organs 289.* > 2006 ICD-9-CM Diagnosis 289.7
MethemoglobinemiaView the most recent version of ICD-9-CM 289.7 - A morbid condition due to the presence of sulfmethemoglobin in the blood. It is marked by persistent cyanosis, but the blood count does not reveal any special abnormality in the blood. It is thought to be caused by the action of hydrogen sulfide absorbed from the intestine.
- The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin M (an autosomal dominant trait).
- 289.7 is a specific code that can be used to specify a diagnosis
- 289.7 contains 21 index entries
- View the ICD-9-CM Volume 1 289.* hierarchy
Alternate Terminology- Congenital NADH [DPNH]-methemoglobin-reductase deficiency
- Hemoglobin M [Hb-M] disease
- Methemoglobinemia:
- NOS
- acquired (with sulfhemoglobinemia)
- hereditary
- toxic
- Stokvis' disease
- Sulfhemoglobinemia
Index entries containing 289.7:
- Cyanosis 782.5
- autotoxic
289.7 - enterogenous
289.7 Deficiency, deficient- NADH (DPNH) -methemoglobin-reductase (congenital)
289.7 - NADH diaphorase or reductase (congenital)
289.7 Disease, diseased - see also Syndrome- diaphorase deficiency
289.7 - hemoglobin (Hb) 282.7
- M
289.7
- Stokvis (-Talma) (enterogenous cyanosis)
289.7 - van den Bergh's (enterogenous cyanosis)
289.7 Enterogenous cyanosis 289.7Methemoglobinemia 289.7- acquired (with sulfhemoglobinemia)
289.7 - congenital
289.7 - enzymatic
289.7 - Hb-M disease
289.7 - hereditary
289.7 - toxic
289.7 Sensitivity, sensitization - see also Allergy- methemoglobin
289.7 Stokvis' (-Talma) disease (enterogenous cyanosis) 289.7Sulfhemoglobinemia, sulphemoglobinemia (acquired) (congenital) 289.7Syndrome - see also Disease- Stokvis-Talma (enterogenous cyanosis)
289.7 van den Bergh's disease (enterogenous cyanosis) 289.7
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