2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > Iron Deficiency Anemias 280.* >
 2007 ICD-9-CM Diagnosis 280.8
Other specified iron deficiency anemias 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 Therefore, this code may be out of date.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 280.8 can be accessed here. - A syndrome of DYSPHAGIA with IRON-DEFICIENCY ANEMIA that is due to congenital anomalies in the ESOPHAGUS (such as cervical esophageal webs). It is known as Patterson-Kelly syndrome in the United Kingdom.
- 280.8 is a specific code that can be used to specify a diagnosis
- 280.8 contains 17 index entries
- View the ICD-9-CM Volume 1 280.* hierarchy
280.8 also known as:- Paterson-Kelly syndrome
- Plummer-Vinson syndrome
- Sideropenic dysphagia
Index entries containing 280.8:- Anemia 285.9
- deficiency 281.9
- iron (Fe) 280.9
- specified NEC
 280.8
- iron (Fe) deficiency 280.9
- specified NEC 280.8
Dysphagia 787.2- sideropenic 280.8
Kelly (-Patterson) syndrome (sideropenic dysphagia) 280.8
Paterson's syndrome (sideropenic dysphagia) 280.8
Paterson (-Brown) (-Kelly) syndrome (sideropenic dysphagia) 280.8
Paterson-Kelly syndrome or web (sideropenic dysphagia) 280.8
Plummer-Vinson syndrome (sideropenic dysphagia) 280.8
Syndrome - see also Disease- Kelly's (sideropenic dysphagia) 280.8
- Paterson (-Brown) (-Kelly) (sideropenic dysphagia) 280.8
- Plummer-Vinson (sideropenic dysphagia) 280.8
- sideropenic 280.8
- Vinson-Plummer (sideropenic dysphagia) 280.8
- Waldenström-Kjellberg (sideropenic dysphagia) 280.8
Vinson-Plummer syndrome (sideropenic dysphagia) 280.8
Waldenström-Kjellberg syndrome (sideropenic dysphagia) 280.8
Web, webbed (congenital) - see also Anomaly, specified type NEC- Paterson-Kelly (sideropenic dysphagia) 280.8
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