Deficiency of N-glycanase 1
Mannose-6-phosphate isomerase congenital disorder of glycosylation
COG6-CGD - component of oligomeric golgi complex 6-congenital disorder of glycosylation
Alpha-N-acetylgalactosaminidase deficiency
NAGA (alpha-N-acetylgalactosaminidase) deficiency
Carbohydrate deficient glycoprotein syndrome type IId
MGAT2-CDG - alpha-1,6-mannosyl-glycoprotein beta-1,2-n-acetylglucosaminyltransferase congenital disorder of glycosylation
Carbohydrate deficient glycoprotein syndrome
Edema due to hypoproteinemia
NAGA (alpha-N-acetylgalactosaminidase) deficiency type 1
Congenital disorder of glycosylation type 1a
Disorder of sialic acid metabolism
Alpha-N-acetylgalactosaminidase deficiency type 3
Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation
Congenital disorder of glycosylation type 2d
Alpha-2-antitrypsin deficiency
Congenital disorder of glycosylation type IIa
Congenital disorder of glycosylation type 1b
Congenital disorder of glycosylation type 1z
Carbohydrate deficiency glycoprotein syndrome
Component of oligomeric golgi complex 2-related congenital disorder of glycosylation
CDG - Carbohydrate-deficient glycoprotein syndrome type III
NAGA (alpha-N-acetylgalactosaminidase) deficiency type 3
CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation
Carbohydrate deficient glycoprotein syndrome type 2d
Mannosephosphate isomerase congenital disorder of glycosylation
Carbohydrate deficient glycoprotein syndrome type Ia
CDG - Carbohydrate-deficient glycoprotein syndrome
Congenital disorder of glycosylation type IIk
Transmembrane protein 199 congenital disorder of glycosylation
Congenital disorder of glycosylation type 2l
CDG - Carbohydrate-deficient glycoprotein syndrome type II
Congenital disorder of glycosylation type IIL
PMM2-CDG (congenital disorder of glycosylation)
TMEM199 congenital disorder of glycosylation
Carbohydrate-deficient glycoprotein syndrome type I
Carbohydrate deficient glycoprotein syndrome type Iz
Carbohydrate-deficient glycoprotein syndrome
NGLY1-congenital disorder of deglycosylation
Normocytic anaemia
CDG1M - carbohydrate deficient glycoprotein syndrome type 1m
Carbohydrate deficient glycoprotein syndrome type 1o
Carbohydrate deficient glycoprotein syndrome type 2k
Schindler disease type 2
Carbohydrate deficient glycoprotein syndrome type Ib
Schindler disease
Schindler disease type 1
TMEM165-CDG - transmembrane protein 165 congenital disorder of glycosylation
Congenital disorder of glycosylation type 2k
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
Carbohydrate deficient glycoprotein syndrome type IIk
Pulmonary edema due to hypoproteinemia
Transmembrane protein 165 congenital disorder of glycosylation
Component of oligomeric golgi complex 6-congenital disorder of glycosylation
Congenital disorder of glycosylation type 2a
Carbohydrate deficient glycoprotein syndrome type IIp
Alpha-N-acetylgalactosaminidase deficiency type 2
B4GALT1-CDG - Beta-1,4-galactosyltransferase deficiency congenital disorder of glycosylation
Congenital disorder of glycosylation type 1o
N-Acetylglucosaminyl transferase II deficiency
Normocytic anemia
Alacrimia, choreoathetosis, liver dysfunction syndrome
Congenital disorder of glycosylation type II due to MAN1B1 deficiency
MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation
DPM3-CDG - dolichyl-phosphate mannosyltransferase 3 congenital disorder of glycosylation
TMEM199-CDG - transmembrane protein 199 congenital disorder of glycosylation
Alpha-N-acetylgalactosaminidase deficiency type 1
N-glycanase 1 congenital disorder of deglycosylation
CDG - Carbohydrate-deficient glycoprotein syndrome type I
Carbohydrate-deficient glycoprotein syndrome type II
Congenital disorder of glycosylation
COG2-related congenital disorder of glycosylation
Congenital disorder of glycosylation type IId
Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1
MPI-CDG - mannosephosphate isomerase congenital disorder of glycosylation
NAGA (alpha-N-acetylgalactosaminidase) deficiency type 2
Carbohydrate deficient glycoprotein syndrome type 1m
Carbohydrate-deficient glycoprotein syndrome type III
Schindler disease type 3
CDG (congenital disorder of glycosylation) syndrome type IIp
Oedema due to hypoproteinaemia
Glycoprotein storage disorder
Carbohydrate deficient glycoprotein syndrome type 2a
Congenital disorder of glycosylation type IIp
Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency
COG2-CDG - component of oligomeric golgi complex 2 - congenital disorder of glycosylation
Carbohydrate deficient glycoprotein syndrome type IIa
Carbohydrate deficient glycoprotein syndrome type Im
Congenital disorder of glycosylation type Ia
Pulmonary oedema due to hypoproteinaemia
Beta-1,4-galactosyltransferase deficiency

Frequently Asked Questions

What is the ICD-10 code for other disorders of glycoprotein metabolism?

The ICD-10-CM code for other disorders of glycoprotein metabolism is E77.8. The full clinical description is "Other disorders of glycoprotein metabolism". E77.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E77.8 mean?

ICD-10-CM code E77.8 represents “Other disorders of glycoprotein 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 E77.8 a billable code?

Yes, E77.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E77.8 in?

E77.8 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E77.8?

E77.8 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 E77.8 map to?

E77.8 maps to 28 SNOMED CT concepts: 768846004, 312857009, 238048001, 879937000, 880065001, and 23 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E77.8?

E77.8 is linked to 1 UMLS Concept Unique Identifier: C0348493. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E77.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of glycoprotein 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 E77.8?

E77.8 maps to the ICD-11 code: 5C56.2Z (Glycoproteinosis, unspecified).

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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.