E88.09
BillableOth disorders of plasma-protein metabolism, NEC
Other disorders of plasma-protein metabolism, not elsewhere classified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Bisalbuminemia
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •histiocytosis X (chronic)C96.6
- •monoclonal gammopathy (of undetermined significance)D47.2
- •polyclonal hypergammaglobulinemiaD89.0
- •Waldenström macroglobulinemiaC88.00
Excludes 2
Conditions not included here, but the patient may have both
Use Additional Code
Additional codes that should follow this code
- codes for associated conditions
Also Known As / Clinical Terms(90)
SNOMED CT
- Hypoproteinaemia8900005
- Hypoproteinemia8900005
- Autosomal variant form of transthyretin25067009
- Hyperproteinaemia37064009
- Hyperproteinemia37064009
- Congenital atransferrinaemia111571009
- Congenital atransferrinemia111571009
- Hypoalbuminaemia119247004
- Hypoalbuminemia119247004
- Serum albumin low119247004
- Hyperalbuminaemia119248009
- Hyperalbuminemia119248009
- Bisalbuminaemia123806003
- Bisalbuminemia123806003
- Double albuminaemia123806003
- Double albuminemia123806003
- Analbuminaemia129232009
- Analbuminemia129232009
- Neuropathy associated with dysproteinaemias230585004
- Neuropathy associated with dysproteinemias230585004
- Congenital transferrin deficiency234353009
- Alpha-1-antichymotrypsin deficiency235909002
- Antichymotrypsin deficiency-alpha-1235909002
- Hypoalbuminaemic ascites236006000
- Hypoalbuminemic ascites236006000
- Metabolic ascites236006000
- Deficiency of choline esterase II (unspecific)360631004
- Deficiency of inosinase360878001
- Deficiency of inosine nucleosidase360878001
- Disorder of protein metabolism363090004
- Macroamylasaemia416676005
- Macroamylasemia416676005
- Congenital analbuminaemia718721006
- Congenital analbuminemia718721006
- Edema due to hypoproteinemia1254950004
- Oedema due to hypoproteinaemia1254950004
- Hereditary butyrylcholinesterase deficiency1296959007
- Hereditary pseudocholinesterase deficiency1296959007
- Disorder of plasma protein metabolism147211000119101
- Hypoalbuminaemia due to protein calorie malnutrition97361000119109
- Hypoalbuminemia due to protein calorie malnutrition97361000119109
UMLS
Clinical Terms
- Hypoalbuminaemia due to protein calorie malnutrition
- Hypoalbuminemia due to protein calorie malnutrition
- Bisalbuminemia (finding)
- Congenital transferrin deficiency
- Alpha-1-antichymotrypsin deficiency
- Serum albumin low
- Double albuminemia
- Deficiency of choline esterase II (unspecific)
- Autosomal variant form of transthyretin
- Congenital atransferrinemia
- Analbuminemia
- Macroamylasemia
- Bisalbuminaemia
- Disorder of protein metabolism
- Edema due to hypoproteinemia
- Hyperalbuminaemia
- Double albuminaemia
- Congenital analbuminemia
- Hyperproteinaemia
- Hypoalbuminemic ascites
- Hyperproteinemia
- Analbuminaemia
- Deficiency of inosine nucleosidase
- Hypoproteinaemia
- Metabolic ascites
- Macroamylasaemia
- Neuropathy associated with dysproteinaemias
- Oedema due to hypoproteinaemia
- Congenital atransferrinaemia
- Antichymotrypsin deficiency-alpha-1
- Neuropathy associated with dysproteinemias
- Hereditary butyrylcholinesterase deficiency
- Hereditary pseudocholinesterase deficiency
- Hypoalbuminaemic ascites
- Hypoproteinemia
- Deficiency of inosinase
- Congenital analbuminaemia
- Disorder of plasma protein metabolism
- Hypoalbuminemia
- Hyperalbuminemia
- Bisalbuminemia
- Hypoalbuminaemia
Frequently Asked Questions
What is the ICD-10 code for oth disorders of plasma-protein metabolism, nec?
The ICD-10-CM code for oth disorders of plasma-protein metabolism, nec is E88.09. The full clinical description is "Other disorders of plasma-protein metabolism, not elsewhere classified". E88.09 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E88.09 mean?
ICD-10-CM code E88.09 represents “Other disorders of plasma-protein metabolism, not elsewhere classified”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E88.09 a billable code?
Yes, E88.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E88.09 in?
E88.09 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E88.09?
E88.09 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 7 more.
Are additional codes required with E88.09?
Yes, when using E88.09, also report: codes for associated conditions.
What SNOMED CT codes does E88.09 map to?
E88.09 maps to 21 SNOMED CT concepts: 235909002, 129232009, 25067009, 123806003, 718721006, and 16 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E88.09?
E88.09 is linked to 2 UMLS Concept Unique Identifiers: C1261565, C2874311. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E88.09 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth disorders of plasma-protein metabolism, nec affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E88.09?
There is no direct ICD-11 mapping available for E88.09 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.