E77.1
BillableDefects in glycoprotein degradation
Defects in glycoprotein degradation
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Aspartylglucosaminuria
- Fucosidosis
- Mannosidosis
- Sialidosis [mucolipidosis I]
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Dysmorphic sialidosis, congenital form27642008
- Combined deficiency of neuroaminidase and beta galactosidase35691006
- Combined deficiency of sialidase AND beta galactosidase35691006
- GSL - Galactosialidosis35691006
- Galactosialidosis35691006
- Goldberg syndrome35691006
- Neuraminidase deficiency with beta-galactosidase deficiency35691006
- Protective protein deficiency35691006
- Mucolipidosis I38795005
- Mucolipidosis type I38795005
- Mucolipidosis, type I38795005
- Neuraminidase deficiency38795005
- Neuroaminidase deficiency38795005
- Sialidase deficiency38795005
- Sialidosis38795005
- Dysmorphic sialidosis, infantile form51984006
- Dysmorphic sialidosis52186006
- Sialidosis, type 252186006
- Aspartylglucosaminuria54954004
- Aspartylglycosaminuria54954004
- Juvenile mannosidosis58112007
- Mannosidosis, juvenile-adult onset58112007
- Mannosidosis, mild form58112007
- Mannosidosis, type II58112007
- Fucosidosis type I61172008
- Fucosidosis, fatal infantile type61172008
- Fucosidosis, type I61172008
- Infantile fucosidosis61172008
- Infantile mannosidosis62311004
- Mannosidosis infantile onset62311004
- Mannosidosis, severe form62311004
- Mannosidosis, type I62311004
- Alpha-L-fucosidase deficiency64716005
- Fucosidase deficiency64716005
- Fucosidosis64716005
- alpha-L-fucosidase deficiency64716005
- Alpha-D-mannosidosis65524005
- Alpha-mannosidase deficiency65524005
- Mannosidosis65524005
- alpha-Mannosidase deficiency65524005
- Mucolipidosis70528007
- Dysmorphic sialidosis with renal involvement81896006
- Nephrosialidosis81896006
- Dysmorphic sialidosis, juvenile form111383007
- Beta-D-mannosidosis238047006
- Beta-mannosidase deficiency238047006
- Childhood fucosidosis399045007
- Fucosidosis type II399045007
- Fucosidosis, juvenile form399045007
- Fucosidosis, type II399045007
- Juvenile fucosidosis399045007
- Adult fucosidosis399249008
- Cherry red spot myoclonus syndrome723675006
- Lipomucopolysaccharidosis723675006
- Normomorphic sialidosis723675006
- Sialidosis type 1723675006
- Oligosaccharidosis1155842003
- Myoclonic disorder due to sialidosis1263503005
UMLS
- AGA DEFICIENCYC0268225
- AGA DeficienciesC0268225
- AGA DeficiencyC0268225
- AGUC0268225
- ASPARTYLGLUCOSAMINIDASE DEFICIENCYC0268225
- ASPARTYLGLUCOSAMINURIAC0268225
- ASPARTYLGLYCOSAMINURIAC0268225
- Aspartylglucosamidase DeficienciesC0268225
- Aspartylglucosamidase DeficiencyC0268225
- AspartylglucosaminuriaC0268225
- Aspartylglucosaminuria (disorder)C0268225
- AspartylglucosaminuriasC0268225
- AspartylglycosaminuriaC0268225
- AspartylglycosaminuriasC0268225
- Deficiencies, AGAC0268225
- Deficiencies, AspartylglucosamidaseC0268225
- Deficiencies, GlycoasparaginaseC0268225
- Deficiency, AGAC0268225
- Deficiency, AspartylglucosamidaseC0268225
- Deficiency, GlycoasparaginaseC0268225
- GLYCOASPARAGINASEC0268225
- Glycoasparaginase DeficienciesC0268225
- Glycoasparaginase DeficiencyC0268225
- aspartylglucosaminuriaC0268225
- aspartylglycosaminuriaC0268225
- ALPHA FUCOSIDASE DEFIC DISC0016788
- ALPHA L FUCOSIDASE DEFIC DISC0016788
- ALPHA-L-FUCOSIDASE DEFICIENCYC0016788
- Alpha-Fucosidase DeficiencyC0016788
- Alpha-L-fucosidase deficiencyC0016788
- DEFIC DIS ALPHA FUCOSIDASEC0016788
- DEFIC DIS ALPHA L FUCOSIDASEC0016788
- Deficiency Disease, FucosidaseC0016788
- Deficiency Disease, alpha FucosidaseC0016788
- Deficiency Disease, alpha L FucosidaseC0016788
- Deficiency Disease, alpha-FucosidaseC0016788
- Deficiency Disease, alpha-L-FucosidaseC0016788
- Deficiency Diseases, FucosidaseC0016788
- Deficiency Diseases, alpha-FucosidaseC0016788
- Deficiency Diseases, alpha-L-FucosidaseC0016788
- Disease, Fucosidase DeficiencyC0016788
- Disease, alpha-Fucosidase DeficiencyC0016788
- Disease, alpha-L-Fucosidase DeficiencyC0016788
- Diseases, Fucosidase DeficiencyC0016788
- Diseases, alpha-Fucosidase DeficiencyC0016788
- Diseases, alpha-L-Fucosidase DeficiencyC0016788
- FUCOSIDASE DEFIC DISC0016788
- FUCOSIDOSISC0016788
- Fucosidase DeficiencyC0016788
- Fucosidase Deficiency DiseaseC0016788
- Fucosidase Deficiency DiseasesC0016788
- Fucosidase deficiencyC0016788
- FucosidosisC0016788
- Fucosidosis (disorder)C0016788
- alpha Fucosidase Deficiency DiseaseC0016788
- alpha L Fucosidase Deficiency DiseaseC0016788
- alpha fucosidase deficiencyC0016788
- alpha-Fucosidase Deficiency DiseaseC0016788
- alpha-Fucosidase Deficiency DiseasesC0016788
- alpha-L-Fucosidase DeficiencyC0016788
- alpha-L-Fucosidase Deficiency DiseaseC0016788
- alpha-L-Fucosidase Deficiency DiseasesC0016788
- alpha-L-fucosidase deficiencyC0016788
- fucosidosisC0016788
- CHERRY RED SPOT--MYOCLONUS SYNDROMEC0268226
- Cherry Red Spot Myoclonus SyndromeC0268226
- Cherry Red Spot-Myoclonus SyndromeC0268226
- Cherry red spot myoclonus syndromeC0268226
- Deficiencies, Glycoprotein NeuraminidaseC0268226
- Deficiency, Glycoprotein NeuraminidaseC0268226
- Glycoprotein Neuraminidase DeficienciesC0268226
- Glycoprotein Neuraminidase DeficiencyC0268226
- MYOCLONUS--CHERRY RED SPOT SYNDROMEC0268226
- Mucolipidoses, Type IC0268226
- Mucolipidosis IC0268226
- Mucolipidosis Type 1C0268226
- Mucolipidosis Type IC0268226
- Mucolipidosis type IC0268226
- Mucolipidosis, Type IC0268226
- Mucolipidosis, type IC0268226
- Myoclonus Cherry Red Spot SyndromeC0268226
- Myoclonus cherry red spot syndromeC0268226
- Myoclonus-Cherry Red Spot SyndromeC0268226
- Neuraminidase DeficiencyC0268226
- SialidosisC0268226
- Sialidosis (disorder)C0268226
- Sialidosis Type IIC0268226
- Sialidosis [mucolipidosis I]C0268226
- Type I MucolipidosesC0268226
- Type I MucolipidosisC0268226
- mucolipidosis IC0268226
- neuraminidase deficiencyC0268226
- sialidosesC0268226
- sialidosisC0268226
- Defects in glycoprotein degradationC0494342
- Deficiency Disease, MannosidaseC1257960
- Deficiency Diseases, MannosidaseC1257960
- Deficiency Syndrome, MannosidaseC1257960
- Deficiency Syndromes, MannosidaseC1257960
- Diseases, Mannosidase DeficiencyC1257960
- MANNOSIDASE DEFIC DISC1257960
- MANNOSIDASE DEFIC SYNDROMESC1257960
- Mannosidase Deficiency DiseaseC1257960
- Mannosidase Deficiency DiseasesC1257960
- Mannosidase Deficiency SyndromeC1257960
- Mannosidase Deficiency SyndromesC1257960
- MannosidosesC1257960
- MannosidosisC1257960
- Mannosidosis (disorder)C1257960
- mannosidase deficiencyC1257960
- mannosidosisC1257960
Frequently Asked Questions
What is the ICD-10 code for defects in glycoprotein degradation?
The ICD-10-CM code for defects in glycoprotein degradation is E77.1. The full clinical description is "Defects in glycoprotein degradation". E77.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E77.1 mean?
ICD-10-CM code E77.1 represents "Defects in glycoprotein degradation". 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 E77.1 a billable code?
Yes, E77.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E77.1 in?
E77.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E77.1?
E77.1 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 3 more.
What SNOMED CT codes does E77.1 map to?
E77.1 maps to 20 SNOMED CT concepts: 399249008, 65524005, 64716005, 54954004, 238047006, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E77.1?
E77.1 is linked to 5 UMLS Concept Unique Identifiers: C0268225, C0016788, C0268226, C0494342, C1257960. 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.