E74.21
BillableGalactosemia
Galactosemia
Coding Notes
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
- Epimerase deficiency8849004
- GALE (UDP-galactose-4-epimerase) deficiency8849004
- Galactosaemia - epimerase deficiency8849004
- Galactosaemia III8849004
- Galactose epimerase deficiency8849004
- Galactosemia - epimerase deficiency8849004
- Galactosemia III8849004
- UDP (uridine diphosphate) galactose-4-epimerase deficiency8849004
- UDP (uridine diphosphate) glucose-4-epimerase deficiency8849004
- Uridine diphosphate galactose-4 epimerase deficiency8849004
- Uridine diphosphate galactose-4-epimerase deficiency8849004
- Uridine diphosphate glucose-4-epimerase deficiency8849004
- Classical galactosaemia, homozygous Duarte-type10899004
- Classical galactosemia, homozygous Duarte-type10899004
- Classical galactosaemia, heterozygous type41326006
- Classical galactosemia, heterozygous type41326006
- Classical galactosaemia, homozygous Negro-type61451000
- Classical galactosemia, homozygous Negro-type61451000
- Classical galactosaemia124354006
- Classical galactosemia124354006
- Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase124354006
- Deficiency of galactose-1-phosphate uridyl transferase124354006
- Deficiency of hexose-1-phosphate uridylyltransferase124354006
- Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase124354006
- Deficiency of uridyl transferase124354006
- GALT deficiency124354006
- Transferase deficiency galactosaemia124354006
- Transferase deficiency galactosemia124354006
- Galactosaemia190745006
- Galactosemia190745006
- Disorder of galactose metabolism237963003
- Galactose metabolism disorder237963003
- Generalised uridine diphosphate galactose-4-epimerase deficiency297237003
- Generalized uridine diphosphate galactose-4-epimerase deficiency297237003
- Erythrocyte uridine diphosphate galactose-4-epimerase deficiency297238008
- Deficiency of UTP-hexose-1-phosphate uridylyltransferase398664009
- Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase398664009
- UTP-hexose-1-phosphate uridyltransferase deficiency398664009
- Deficiency of galactose mutarotase1187616008
- GALM (galactose mutarotase) deficiency1187616008
- Galactosaemia type 41187616008
- Galactosemia type 41187616008
- Early neonatal jaundice due to galactosaemia1335871007
- Early neonatal jaundice due to galactosemia1335871007
Frequently Asked Questions
What is the ICD-10 code for galactosemia?
The ICD-10-CM code for galactosemia is E74.21. The full clinical description is "Galactosemia". E74.21 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.21 mean?
ICD-10-CM code E74.21 represents "Galactosemia". 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 E74.21 a billable code?
Yes, E74.21 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.21 in?
E74.21 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.21?
E74.21 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 E74.21 map to?
E74.21 maps to 12 SNOMED CT concepts: 124354006, 41326006, 10899004, 61451000, 398664009, and 7 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E74.21?
E74.21 is linked to 1 UMLS Concept Unique Identifier: C0016952. 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.