E77.8
BillableOther disorders of glycoprotein metabolism
Other disorders of glycoprotein metabolism
Coding Notes
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
- Glycoprotein storage disorder7810004
- Alpha-N-acetylgalactosaminidase deficiency238048001
- NAGA (alpha-N-acetylgalactosaminidase) deficiency238048001
- Schindler disease238048001
- CDG - Carbohydrate-deficient glycoprotein syndrome238049009
- Carbohydrate deficiency glycoprotein syndrome238049009
- Carbohydrate deficient glycoprotein syndrome238049009
- Carbohydrate-deficient glycoprotein syndrome238049009
- Congenital disorder of glycosylation238049009
- Disorder of sialic acid metabolism238050009
- CDG - Carbohydrate-deficient glycoprotein syndrome type I277893002
- Carbohydrate-deficient glycoprotein syndrome type I277893002
- CDG - Carbohydrate-deficient glycoprotein syndrome type II277894008
- Carbohydrate-deficient glycoprotein syndrome type II277894008
- N-Acetylglucosaminyl transferase II deficiency277894008
- CDG - Carbohydrate-deficient glycoprotein syndrome type III277895009
- Carbohydrate-deficient glycoprotein syndrome type III277895009
- Normocytic anaemia300980002
- Normocytic anemia300980002
- Alpha-2-antitrypsin deficiency312857009
- Carbohydrate deficient glycoprotein syndrome type Ia459063003
- Congenital disorder of glycosylation type 1a459063003
- Congenital disorder of glycosylation type Ia459063003
- PMM2-CDG (congenital disorder of glycosylation)459063003
- Pulmonary edema due to hypoproteinemia700458001
- Pulmonary oedema due to hypoproteinaemia700458001
- CDG1M - carbohydrate deficient glycoprotein syndrome type 1m718712005
- Carbohydrate deficient glycoprotein syndrome type 1m718712005
- Carbohydrate deficient glycoprotein syndrome type Im718712005
- Carbohydrate deficient glycoprotein syndrome type 2a724142005
- Carbohydrate deficient glycoprotein syndrome type IIa724142005
- Congenital disorder of glycosylation type 2a724142005
- Congenital disorder of glycosylation type IIa724142005
- MGAT2-CDG - alpha-1,6-mannosyl-glycoprotein beta-1,2-n-acetylglucosaminyltransferase congenital disorder of glycosylation724142005
- Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency724344004
- Carbohydrate deficient glycoprotein syndrome type 1o725044000
- Congenital disorder of glycosylation type 1o725044000
- DPM3-CDG - dolichyl-phosphate mannosyltransferase 3 congenital disorder of glycosylation725044000
- B4GALT1-CDG - Beta-1,4-galactosyltransferase deficiency congenital disorder of glycosylation725587007
- Beta-1,4-galactosyltransferase deficiency725587007
- Carbohydrate deficient glycoprotein syndrome type 2d725587007
- Carbohydrate deficient glycoprotein syndrome type IId725587007
- Congenital disorder of glycosylation type 2d725587007
- Congenital disorder of glycosylation type IId725587007
- Carbohydrate deficient glycoprotein syndrome type 2k732252005
- Carbohydrate deficient glycoprotein syndrome type IIk732252005
- Congenital disorder of glycosylation type 2k732252005
- Congenital disorder of glycosylation type IIk732252005
- TMEM165-CDG - transmembrane protein 165 congenital disorder of glycosylation732252005
- Transmembrane protein 165 congenital disorder of glycosylation732252005
- Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1733450008
- Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency733450008
- Congenital disorder of glycosylation type II due to MAN1B1 deficiency733450008
- MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation733450008
- Alacrimia, choreoathetosis, liver dysfunction syndrome768846004
- Deficiency of N-glycanase 1768846004
- N-glycanase 1 congenital disorder of deglycosylation768846004
- NGLY1-congenital disorder of deglycosylation768846004
- Alpha-N-acetylgalactosaminidase deficiency type 1879937000
- NAGA (alpha-N-acetylgalactosaminidase) deficiency type 1879937000
- Schindler disease type 1879937000
- Alpha-N-acetylgalactosaminidase deficiency type 2880065001
- NAGA (alpha-N-acetylgalactosaminidase) deficiency type 2880065001
- Schindler disease type 2880065001
- Alpha-N-acetylgalactosaminidase deficiency type 3880066000
- NAGA (alpha-N-acetylgalactosaminidase) deficiency type 3880066000
- Schindler disease type 3880066000
- COG2-CDG - component of oligomeric golgi complex 2 - congenital disorder of glycosylation1197753005
- COG2-related congenital disorder of glycosylation1197753005
- Component of oligomeric golgi complex 2-related congenital disorder of glycosylation1197753005
- CDG (congenital disorder of glycosylation) syndrome type IIp1208738002
- Carbohydrate deficient glycoprotein syndrome type IIp1208738002
- Congenital disorder of glycosylation type IIp1208738002
- TMEM199 congenital disorder of glycosylation1208738002
- TMEM199-CDG - transmembrane protein 199 congenital disorder of glycosylation1208738002
- Transmembrane protein 199 congenital disorder of glycosylation1208738002
- COG6-CGD - component of oligomeric golgi complex 6-congenital disorder of glycosylation1220574003
- Component of oligomeric golgi complex 6-congenital disorder of glycosylation1220574003
- Congenital disorder of glycosylation type 2l1220574003
- Congenital disorder of glycosylation type IIL1220574003
- Carbohydrate deficient glycoprotein syndrome type Ib1231141008
- Congenital disorder of glycosylation type 1b1231141008
- MPI-CDG - mannosephosphate isomerase congenital disorder of glycosylation1231141008
- Mannose-6-phosphate isomerase congenital disorder of glycosylation1231141008
- Mannosephosphate isomerase congenital disorder of glycosylation1231141008
- CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation1237417007
- Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation1237417007
- Carbohydrate deficient glycoprotein syndrome type Iz1237417007
- Congenital disorder of glycosylation type 1z1237417007
- Edema due to hypoproteinemia1254950004
- Oedema due to hypoproteinaemia1254950004
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.
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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.