E74.21 Generalized uridine diphosphate galactose-4-epimerase deficiency

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Generalized uridine diphosphate galactose-4-epimerase deficiency

Generalized uridine diphosphate galactose-4-epimerase deficiency
Synonym for Galactosemia

    E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)|E70-E88 Metabolic disorders (E70-E88)|E74 Other disorders of carbohydrate metabolism|E74.2 Disorders of galactose metabolism

Results for Generalized uridine diphosphate galactose-4-epimerase deficiency and additional synonyms


E74.21
Galactosemia

Synonyms:

Classical galactosaemia|Classical galactosaemia, heterozygous type|Classical galactosaemia, homozygous Duarte-type|Classical galactosaemia, homozygous Negro-type|Classical galactosemia|Classical galactosemia, heterozygous type|Classical galactosemia, heterozygous type (disorder)|Classical galactosemia, homozygous Duarte-type|Classical galactosemia, homozygous Duarte-type (disorder)|Classical galactosemia, homozygous Negro-type|Classical galactosemia, homozygous Negro-type (disorder)|Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase|Deficiency of galactose-1-phosphate uridyl transferase|Deficiency of hexose-1-phosphate uridylyltransferase|Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase|Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase (disorder)|Deficiency of uridyl transferase|Epimerase deficiency|Erythrocyte uridine diphosphate galactose-4-epimerase deficiency|Erythrocyte uridine diphosphate galactose-4-epimerase deficiency (disorder)|GALE|GALT deficiency|Galactosaemia|Galactosaemia - epimerase deficiency|Galactosaemia III|Galactose epimerase deficiency|Galactosemia (disorder)|Galactosemia - epimerase deficiency|Galactosemia III|Generalised uridine diphosphate galactose-4-epimerase deficiency|Generalized uridine diphosphate galactose-4-epimerase deficiency|Generalized uridine diphosphate galactose-4-epimerase deficiency (disorder)|Perinatal jaundice due to galactosaemia|Perinatal jaundice due to galactosemia|Perinatal jaundice due to galactosemia (disorder)|Transferase deficiency galactosaemia|Transferase deficiency galactosemia|UDPgalactose-4-epimerase deficiency|UDPglucose-4-epimerase deficiency|Uridine diphosphate (UDP) glucose-4-epimerase deficiency|Uridine diphosphate galactose-4 epimerase deficiency|Uridine diphosphate galactose-4-epimerase deficiency|Uridine diphosphate glucose-4-epimerase deficiency|Uridine diphosphate glucose-4-epimerase deficiency (disorder)

Subcategories:

    All content of the ICD-10 CM Search is based on the classifications and codes of the Centers for Medicare and Medicaid Services (CMS) and the National Center for Health Statistics (NCHS). The accumulation of synonyms is carried out by Averbis GmbH with Healthcare Natural Language Processing. All information is provided without guarantee. Errors and omissions excepted. We expressly reserve the right to make changes, additions or deletions to the information or links provided at any time without prior notice. Our offer is non-binding. For correctness, completeness and topicality or designations no liability is assumed.

    ICD-Search ICD 10 CM (Clinical Modification) 2017 through Healthcare Natural Language Processing & Deep Learning

    ICD-Code / International Statistical Classification of Diseases and Related Health Problems (ICD) for: Generalized uridine diphosphate galactose-4-epimerase deficiency

    ICD Code for Disease, Diagnosis E74.21

    ICD Code an Classification Galactosemia

    Chapter, Outline, Main Categories, Parent Concepts or Top Concepts: E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)|E70-E88 Metabolic disorders (E70-E88)|E74 Other disorders of carbohydrate metabolism|E74.2 Disorders of galactose metabolism

    Subcategories, subconcepts or child concepts:

    Synonyms:

    Synonyms: E74.21: Generalized uridine diphosphate galactose-4-epimerase deficiency

    Other Synonyms of the Category: Classical galactosaemia|Classical galactosaemia, heterozygous type|Classical galactosaemia, homozygous Duarte-type|Classical galactosaemia, homozygous Negro-type|Classical galactosemia|Classical galactosemia, heterozygous type|Classical galactosemia, heterozygous type (disorder)|Classical galactosemia, homozygous Duarte-type|Classical galactosemia, homozygous Duarte-type (disorder)|Classical galactosemia, homozygous Negro-type|Classical galactosemia, homozygous Negro-type (disorder)|Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase|Deficiency of galactose-1-phosphate uridyl transferase|Deficiency of hexose-1-phosphate uridylyltransferase|Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase|Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase (disorder)|Deficiency of uridyl transferase|Epimerase deficiency|Erythrocyte uridine diphosphate galactose-4-epimerase deficiency|Erythrocyte uridine diphosphate galactose-4-epimerase deficiency (disorder)|GALE|GALT deficiency|Galactosaemia|Galactosaemia - epimerase deficiency|Galactosaemia III|Galactose epimerase deficiency|Galactosemia (disorder)|Galactosemia - epimerase deficiency|Galactosemia III|Generalised uridine diphosphate galactose-4-epimerase deficiency|Generalized uridine diphosphate galactose-4-epimerase deficiency|Generalized uridine diphosphate galactose-4-epimerase deficiency (disorder)|Perinatal jaundice due to galactosaemia|Perinatal jaundice due to galactosemia|Perinatal jaundice due to galactosemia (disorder)|Transferase deficiency galactosaemia|Transferase deficiency galactosemia|UDPgalactose-4-epimerase deficiency|UDPglucose-4-epimerase deficiency|Uridine diphosphate (UDP) glucose-4-epimerase deficiency|Uridine diphosphate galactose-4 epimerase deficiency|Uridine diphosphate galactose-4-epimerase deficiency|Uridine diphosphate glucose-4-epimerase deficiency|Uridine diphosphate glucose-4-epimerase deficiency (disorder)

    ICD 10 CM 2017, (Clinical Modification) for coding of death certificates and mortality data. The international Statistical Classification of Diseases and Related Health Problems (ICD) 10th Revision and Clinical Modification. International Classification of Diseases, Tenth Revision, Clinical Modification.E74.21 Galactosemia and Generalized uridine diphosphate galactose-4-epimerase deficiency

    Generalized uridine diphosphate galactose-4-epimerase deficiency
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