E74.29
BillableOther disorders of galactose metabolism
Other disorders of galactose metabolism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Galactokinase deficiency
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
- •diabetes mellitusE08-E13
- •hypoglycemia NOSE16.2
- •increased secretion of glucagonE16.3
- •mucopolysaccharidosisE76.0-E76.3
Related Codes(2)
Also Known As / Clinical Terms(97)
SNOMED CT
- Galactosuria71690006
- Deficiency of galactose dehydrogenase124133008
- Deficiency of galactokinase124302001
- GALK (galactokinase) deficiency124302001
- Galactokinase deficiency124302001
- Galactokinase deficiency galactosaemia124302001
- Galactokinase deficiency galactosemia124302001
- Galactosaemia - galactokinase deficiency124302001
- Galactosaemia II124302001
- Galactosemia - galactokinase deficiency124302001
- Galactosemia II124302001
- Deficiency of beta-galactosidase124465002
- Galactosaemia190745006
- Galactosemia190745006
- Disorder of galactose metabolism237963003
- Galactose metabolism disorder237963003
UMLS
- DEFIC DIS GALACTOKINASEC0268155
- Deficiencies, GALKC0268155
- Deficiencies, GalactokinaseC0268155
- Deficiencies, Hereditary GalactokinaseC0268155
- Deficiency Disease, GalactokinaseC0268155
- Deficiency of galactokinaseC0268155
- Deficiency of galactokinase (disorder)C0268155
- Deficiency, GALKC0268155
- Deficiency, GalactokinaseC0268155
- Deficiency, Hereditary GalactokinaseC0268155
- GALAC2C0268155
- GALACTOKINASE DEFIC DISC0268155
- GALACTOKINASE DEFICIENCYC0268155
- GALACTOSEMIA IIC0268155
- GALK (galactokinase) deficiencyC0268155
- GALK DEFICIENCYC0268155
- GALK DeficienciesC0268155
- GALK DeficiencyC0268155
- GALK deficiencyC0268155
- Galactokinase DeficienciesC0268155
- Galactokinase Deficiencies, HereditaryC0268155
- Galactokinase DeficiencyC0268155
- Galactokinase Deficiency DiseaseC0268155
- Galactokinase Deficiency DiseasesC0268155
- Galactokinase Deficiency, HereditaryC0268155
- Galactokinase deficiencyC0268155
- Galactokinase deficiency diseaseC0268155
- Galactokinase deficiency galactosaemiaC0268155
- Galactokinase deficiency galactosemiaC0268155
- Galactosaemia - galactokinase deficiencyC0268155
- Galactosaemia IIC0268155
- Galactosemia - galactokinase deficiencyC0268155
- Galactosemia 2C0268155
- Galactosemia 2sC0268155
- Galactosemia IIC0268155
- Galactosemia Type 2C0268155
- Hereditary Galactokinase DeficienciesC0268155
- Hereditary Galactokinase DeficiencyC0268155
- galactokinase deficiencyC0268155
- type ii galactosemiaC0268155
- Other disorders of galactose metabolismC2874269
Clinical Terms
- Deficiency of beta-galactosidase
- Galactokinase Deficiencies, Hereditary
- Deficiency, Galactokinase
- Galactokinase deficiency galactosemia
- Galactosemia Type 2
- Hereditary Galactokinase Deficiency
- Galactosemia 2
- galactokinase deficiency
- DEFIC DIS GALACTOKINASE
- Deficiency of galactokinase
- Galactosemia 2s
- Deficiency of galactose dehydrogenase
- Disorder of galactose metabolism
- type ii galactosemia
- GALACTOKINASE DEFIC DIS
- Deficiency, GALK
- GALK deficiency
- Deficiencies, Hereditary Galactokinase
- Galactosaemia
- Galactokinase Deficiency Disease
- Deficiencies, Galactokinase
- Deficiencies, GALK
- Galactokinase Deficiency, Hereditary
- Galactosemia - galactokinase deficiency
- Hereditary Galactokinase Deficiencies
- Deficiency Disease, Galactokinase
- Galactokinase deficiency galactosaemia
- GALK (galactokinase) deficiency
- Galactosemia
- Galactokinase Deficiencies
- Deficiency, Hereditary Galactokinase
- GALK Deficiencies
- Deficiency of galactokinase (disorder)
- Galactokinase Deficiency Diseases
- Galactose metabolism disorder
- GALACTOSEMIA II
- Galactosaemia - galactokinase deficiency
- Galactosuria
- GALAC2
- Galactosaemia II
Frequently Asked Questions
What is the ICD-10 code for other disorders of galactose metabolism?
The ICD-10-CM code for other disorders of galactose metabolism is E74.29. The full clinical description is "Other disorders of galactose metabolism". E74.29 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.29 mean?
ICD-10-CM code E74.29 represents “Other disorders of galactose metabolism”. 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 E74.29 a billable code?
Yes, E74.29 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.29 in?
E74.29 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.29?
E74.29 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.
What SNOMED CT codes does E74.29 map to?
E74.29 maps to 6 SNOMED CT concepts: 124465002, 124302001, 124133008, 237963003, 190745006, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E74.29?
E74.29 is linked to 2 UMLS Concept Unique Identifiers: C0268155, C2874269. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E74.29 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of galactose metabolism 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 E74.29?
There is no direct ICD-11 mapping available for E74.29 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.