2015 ICD-9-CM Diagnosis Code 284.09
Other constitutional aplastic anemia
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- ICD-9-CM 284.09 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 284.09 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
Convert to ICD-10-CM:
284.09 converts directly to:
- 2015/16 ICD-10-CM D61.09 Other constitutional aplastic anemia
Approximate Synonyms
- Acquired Fanconi syndrome
- Anemia, Fanconi
- Congenital hypoplastic anemia
- Constitutional aplastic anemia
- Constitutional aplastic anemia with malformation
- Constitutional red cell aplasia and hypoplasia
- Erythrogenesis imperfecta
- Estren-Dameshek anemia
- Fanconi anemia
- Fanconi's anemia
Clinical Information
- A rare and often fatal inherited disease in which the bone marrow fails to produce red blood cells, white blood cells, platelets, or a combination of these cells. The disease may transform into myelodysplastic syndrome or leukemia
- Fanconi anemia (fa) is an autosomal recessive genetic disorder characterised clinically by progressive bone marrow failure, skeletal deformities and a predisposition to neoplasia. Patient cells manifest an extreme chromosomal instability and hypersensitivity to polyfunctional alkylating agents. It is assumed that the basic defect is related to the repair of dna damage, in particular that of so-called dna crosslinks. Currently there are eight complementation groups in fa (fa-a-fa-h) which indicates that at least eight independent genes can lead to fa. Three of these genes have been identified: fanca, fancc and fancg. (from pmid 10472548)
Applies To
- Fanconi's anemia
- Pancytopenia with malformations
Fanconi's (congenital pancytopenia) 284.09
Fanconi's (congenital pancytopenia) 284.09
