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 newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- diabetes mellitus (E08-E13)
- hypoglycemia NOS (E16.2)
- increased secretion of glucagon (E16.3)
- mucopolysaccharidosis (E76.0-E76.3)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
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
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.
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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.