E13.9
BillableOther specified diabetes mellitus without complications
Other specified diabetes mellitus without complications
Coding Notes
Includes
Conditions included under this code
- diabetes mellitus due to genetic defects of beta-cell function
- diabetes mellitus due to genetic defects in insulin action
- postpancreatectomy diabetes mellitus
- postprocedural diabetes mellitus
- secondary diabetes mellitus NEC
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •diabetes (mellitus) due to autoimmune processE10
- •diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destructionE10
- •diabetes mellitus due to underlying conditionE08
- •drug or chemical induced diabetes mellitusE09
- •gestational diabetesO24.4
- •neonatal diabetes mellitusP70.2
- •type 1 diabetes mellitusE10
Use Additional Code
Additional codes that should follow this code
- code to identify control using:
- •injectable non-insulin antidiabetic drugsZ79.85
- •insulinZ79.4
- •oral antidiabetic drugsZ79.84
- •oral hypoglycemic drugsZ79.84
Related Codes(8)
E13.0Other specified diabetes mellitus with hyperosmolarity
E13.1Other specified diabetes mellitus with ketoacidosis
E13.2Other specified diabetes mellitus with kidney complications
E13.3Oth diabetes mellitus with ophthalmic complications
E13.4Oth diabetes mellitus with neurological complications
E13.5Oth diabetes mellitus with circulatory complications
E13.6Oth diabetes mellitus with other specified complications
E13.8Oth diabetes mellitus with unspecified complications
Related Conditions
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(183)
SNOMED CT
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- Secondary diabetes mellitus8801005
- Diabetes mellitus associated with receptor abnormality42954008
- Neonatal diabetes mellitus49817004
- Diabetes mellitus associated with pancreatic disease51002006
- Pancreatogenic type 3c diabetes mellitus51002006
- Secondary pancreatic diabetes mellitus51002006
- Diabetes mellitus associated with hormonal aetiology59079001
- Diabetes mellitus associated with hormonal etiology59079001
- Congenital hypoplasia of pancreas68591005
- Congenital small pancreas68591005
- Hypoplasia of pancreas68591005
- Pancreatic hypoplasia68591005
- MRDM - malnutrition related diabetes mellitus75524006
- Malnutrition related diabetes mellitus75524006
- Acquired partial lipodystrophy75659004
- Barraquer syndrome75659004
- Barraquer-Simons disease75659004
- Barraquer-Simons syndrome75659004
- Hollander-Simons syndrome75659004
- Lipodystrophic diabetes with partial lipoatrophy75659004
- Macrodystrophia lipomatosa progressiva75659004
- Partial lipoatrophy75659004
- Progressive lipodystrophy75659004
- Progressive partial lipodystrophy75659004
- Diabetes mellitus caused by insulin receptor antibodies75682002
- Mild intellectual development disorder86765009
- Mild intellectual disability86765009
- Mild mental retardation (I.Q. 50-70)86765009
- Mild mental retardation (Intelligence Quotient 50-70)86765009
- Mild mental retardation, IQ in range 50-7086765009
- Diabetes mellitus due to structurally abnormal insulin91352004
- Insulinopathy91352004
- Houssay syndrome123763000
- Houssay's syndrome123763000
- Pre-existing malnutrition-related diabetes mellitus199231005
- Secondary endocrine diabetes mellitus237601000
- Lipodystrophy, partial, with Rieger anomaly, short stature, and insulinopenic diabetes mellitus237608006
- Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes237610008
- Furukawa Takagi Nakao syndrome237611007
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus237611007
- Agenesis of cerebellum253172000
- Congenital absence of cerebellum253172000
- Total agenesis of cerebellum253172000
- MODY - maturity onset diabetes of young609561005
- Maturity-onset diabetes of the young609561005
- HNF4A (hepatocyte nuclear factor 4 alpha) monogenic diabetes mellitus609562003
- MODY1 (maturity onset diabetes of the young type 1)609562003
- Maturity onset diabetes of the young, type 1609562003
- Pre-existing diabetes mellitus in pregnancy609563008
- Permanent diabetes mellitus of infancy609565001
- Permanent neonatal diabetes mellitus609565001
- Diabetes mellitus due to genetic defect in beta cell function609568004
- Diabetes mellitus due to genetic defect in insulin action609569007
- MODY3 (maturity-onset diabetes of the young type 3)609570008
- Maturity-onset diabetes of the young, type 3609570008
- MODY4 (maturity-onset diabetes of the young type 4)609571007
- Maturity-onset diabetes of the young, type 4609571007
- HNF1B (HNF1 homeobox B) monogenic diabetes mellitus609572000
- HNF1B monogenic diabetes mellitus609572000
- HNF1B-MODY - HNF1 homeobox B maturity-onset diabetes of the young type 5609572000
- MODY5 - maturity-onset diabetes of the young type 5609572000
- Maturity-onset diabetes of the young, type 5609572000
- Renal cysts and diabetes syndrome609572000
- MODY6 (maturity-onset diabetes of the young type 6)609573005
- Maturity-onset diabetes of the young, type 6609573005
- MODY7 (maturity-onset diabetes of the young type 7)609574004
- Maturity-onset diabetes of the young, type 7609574004
- Diabetes-pancreatic exocrine dysfunction syndrome609575003
- MODY8 (maturity-onset diabetes of the young type 8)609575003
- Maturity-onset diabetes of the young, type 8609575003
- MODY9 (maturity-onset diabetes of the young type 9)609576002
- Maturity-onset diabetes of the young, type 9609576002
- MODY10 (maturity-onset diabetes of the young type 10)609577006
- Maturity-onset diabetes of the young, type 10609577006
- MODY11 (maturity-onset diabetes of the young type 11)609578001
- Maturity-onset diabetes of the young, type 11609578001
- Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome722206009
- Yorifuji Okuno syndrome722206009
- Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome722454003
- Mental retardation syndrome Belgian type722454003
- Pancreatic and cerebellar agenesis syndrome724067006
- Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome724067006
- Chemical-induced diabetes mellitus737212004
- Diabetes mellitus caused by chemical737212004
- Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome782755007
- Pre-existing malnutrition-related diabetes mellitus in pregnancy1142044000
- ADM - atypical diabetes mellitus530558861000132104
- Atypical diabetes mellitus530558861000132104
UMLS
Clinical Terms
- Hypoplasia of pancreas
- Mental retardation syndrome Belgian type
- MODY10 (maturity-onset diabetes of the young type 10)
- Genetic syndromes of diabetes mellitus
- MODY7 (maturity-onset diabetes of the young type 7)
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
- Congenital hypoplasia of pancreas
- Renal cysts and diabetes syndrome
- Insulinopathy
- Hollander-Simons syndrome
- Secondary pancreatic diabetes mellitus
- Mild intellectual development disorder
- HNF1B monogenic diabetes mellitus
- Diabetes mellitus associated with pancreatic disease
- Pre-existing malnutrition-related diabetes mellitus
- Diabetes mellitus due to genetic defect in beta cell function
- MODY4 (maturity-onset diabetes of the young type 4)
- Maturity-onset diabetes of the young, type 5
- Maturity-onset diabetes of the young, type 3
- MODY9 (maturity-onset diabetes of the young type 9)
- Diabetes mellitus associated with genetic syndrome
- Acquired partial lipodystrophy
- Maturity-onset diabetes of the young, type 6
- Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome
- Maturity-onset diabetes of the young, type 7
- MODY6 (maturity-onset diabetes of the young type 6)
- Lipodystrophic diabetes with partial lipoatrophy
- Mild mental retardation, IQ in range 50-70
- Secondary endocrine diabetes mellitus
- MRDM - malnutrition related diabetes mellitus
- Total agenesis of cerebellum
- MODY11 (maturity-onset diabetes of the young type 11)
- Diabetes mellitus associated with hormonal aetiology
- ADM - atypical diabetes mellitus
- Malnutrition related diabetes mellitus
- Barraquer-Simons disease
- Diabetes mellitus due to genetic defect in insulin action
- Progressive lipodystrophy
- Agenesis of cerebellum
- Barraquer-Simons syndrome
- Diabetes mellitus due to structurally abnormal insulin
- Congenital absence of cerebellum
- Progressive partial lipodystrophy
- Macrodystrophia lipomatosa progressiva
- MODY5 - maturity-onset diabetes of the young type 5
- Houssay syndrome
- Diabetes mellitus associated with receptor abnormality
- Mild mental retardation (I.Q. 50-70)
- Pancreatogenic type 3c diabetes mellitus
- Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes
- Permanent diabetes mellitus of infancy
- Diabetes mellitus caused by chemical
- Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome
- Congenital small pancreas
- Neonatal diabetes mellitus
- Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome
- MODY1 (maturity onset diabetes of the young type 1)
- Pre-existing malnutrition-related diabetes mellitus in pregnancy
- Diabetes mellitus associated with hormonal etiology
- HNF1B-MODY - HNF1 homeobox B maturity-onset diabetes of the young type 5
- Houssay's syndrome
- Maturity-onset diabetes of the young, type 11
- Other Specified Diabetes Mellitus without Complication
- Maturity-onset diabetes of the young
- Maturity-onset diabetes of the young, type 9
- Mild intellectual disability
- HNF4A (hepatocyte nuclear factor 4 alpha) monogenic diabetes mellitus
- Diabetes-pancreatic exocrine dysfunction syndrome
- Atypical diabetes mellitus
- HNF1B (HNF1 homeobox B) monogenic diabetes mellitus
- Diabetes mellitus caused by insulin receptor antibodies
- Maturity onset diabetes of the young, type 1
- Partial lipoatrophy
- Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome
- MODY3 (maturity-onset diabetes of the young type 3)
- Permanent neonatal diabetes mellitus
- Secondary diabetes mellitus
- MODY8 (maturity-onset diabetes of the young type 8)
- Chemical-induced diabetes mellitus
- Pancreatic and cerebellar agenesis syndrome
- Furukawa Takagi Nakao syndrome
- MODY - maturity onset diabetes of young
- Maturity-onset diabetes of the young, type 8
- Pre-existing diabetes mellitus in pregnancy
- Mild mental retardation (Intelligence Quotient 50-70)
- Barraquer syndrome
- Maturity-onset diabetes of the young, type 4
- Yorifuji Okuno syndrome
- Maturity-onset diabetes of the young, type 10
- Pancreatic hypoplasia
- Lipodystrophy, partial, with Rieger anomaly, short stature, and insulinopenic diabetes mellitus
Related ICF Categories(12)
The ICF Core Set for Diabetes Mellitus identifies functioning domains commonly assessed with this condition.
Sensation of pain
Weight maintenance functions
General metabolic functions
Urination functions
Protective functions of the skin
Carrying out daily routine
Walking
Caring for body parts
Looking after one's health
Recreation and leisure
Products or substances for personal consumption
Health services, systems and policies
Showing 12 brief core set categories. The comprehensive core set includes 65 categories.
Frequently Asked Questions
What is the ICD-10 code for other specified diabetes mellitus without complications?
The ICD-10-CM code for other specified diabetes mellitus without complications is E13.9. The full clinical description is "Other specified diabetes mellitus without complications". E13.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E13.9 mean?
ICD-10-CM code E13.9 represents “Other specified diabetes mellitus without complications”. 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 E13.9 a billable code?
Yes, E13.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E13.9 in?
E13.9 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E13.9?
E13.9 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); diabetes (mellitus) due to autoimmune process (E10.-); diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destruction (E10.-); and 5 more.
Are additional codes required with E13.9?
Yes, when using E13.9, also report: control using:; injectable non-insulin antidiabetic drugs (Z79.85); insulin (Z79.4); oral antidiabetic drugs (Z79.84); oral hypoglycemic drugs (Z79.84).
What SNOMED CT codes does E13.9 map to?
E13.9 maps to 41 SNOMED CT concepts: 530558861000132104, 75659004, 237610008, 253172000, 737212004, and 36 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E13.9?
E13.9 is linked to 1 UMLS Concept Unique Identifier: C0494293. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
What ICF functioning codes are related to other specified diabetes mellitus without complications?
The ICF Core Set for Diabetes Mellitus includes 12 functioning categories covering body functions, activities, and environmental factors commonly assessed with this condition. The comprehensive core set includes 65 categories total. Browse the ICF directory.
What is the ICD-11 equivalent of E13.9?
E13.9 maps to the ICD-11 code: 5A13.Y (Diabetes mellitus due to other specified cause).
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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.