E76.22
BillableSanfilippo mucopolysaccharidoses
Sanfilippo mucopolysaccharidoses
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Mucopolysaccharidosis, type III (A) (B) (C) (D)
- Sanfilippo A syndrome
- Sanfilippo B syndrome
- Sanfilippo C syndrome
- Sanfilippo D syndrome
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
- Deficiency of N-acetylglucosamine-6-sulfatase15892005
- Deficiency of N-acetylglucosamine-6-sulphatase15892005
- MPS III-D - Mucopolysaccharidosis III-D15892005
- MPSIIID - Mucopolysaccharidosis type IIID15892005
- Mucopolysaccharidosis III-D15892005
- Mucopolysaccharidosis type IIID15892005
- Mucopolysaccharidosis, MPS-III-D15892005
- N-acetylglucosamine-6-sulfatase deficiency15892005
- N-acetylglucosamine-6-sulphatase deficiency15892005
- Sanfilippo syndrome D15892005
- Sanfilippo syndrome, type D15892005
- Heparan sulfamidase deficiency41572006
- Heparan sulfate sulfatase deficiency41572006
- Heparan sulphamidase deficiency41572006
- Heparan sulphate sulphatase deficiency41572006
- Heparan-N-sulfatase deficiency41572006
- Heparan-N-sulphatase deficiency41572006
- MPS III-A - Mucopolysaccharidosis III-A41572006
- MPSIIIA - Mucopolysaccharidosis type IIIA41572006
- Mucopolysaccharidosis III-A41572006
- Mucopolysaccharidosis type IIIA41572006
- Mucopolysaccharidosis, MPS-III-A41572006
- N-sulfoglucosamine sulfohydrolase deficiency41572006
- N-sulphoglucosamine sulphohydrolase deficiency41572006
- Sanfilippo syndrome A41572006
- Sanfilippo syndrome, type A41572006
- Alpha-N-acetylglucosaminidase deficiency59990008
- MPS III-B - Mucopolysaccharidosis III-B59990008
- MPSIIIB - Mucopolysaccharidosis type IIIB59990008
- Mucopolysaccharidosis III-B59990008
- Mucopolysaccharidosis, MPS-III-B59990008
- N-Acetyl-alpha-D-glucosaminidase deficiency59990008
- Sanfilippo syndrome B59990008
- Sanfilippo syndrome, type B59990008
- alpha-N-acetylglucosaminidase deficiency59990008
- Acetyl-CoA alpha-glucosaminide acetyltransferase deficiency75238000
- Acetyl-CoA: heparan-alpha-D-glucosaminide N-acetyltransferase deficiency75238000
- Heparan-alpha-glucosaminide acetyltransferase deficiency75238000
- MPS III-C - Mucopolysaccharidosis III-C75238000
- MPSIIIC - Mucopolysaccharidosis type IIIC75238000
- Mucopolysaccharidosis III-C75238000
- Mucopolysaccharidosis, MPS-III-C75238000
- N-Acetyl transferase deficiency75238000
- Sanfilippo syndrome C75238000
- Sanfilippo syndrome, type C75238000
- Mucopolysaccharidosis type III88393000
- Mucopolysaccharidosis, MPS-III88393000
- Sanfilippo disease88393000
- Sanfilippo syndrome88393000
UMLS
- ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCYC0086649
- Acetyl CoA:alpha Glucosaminide N Acetyltransferase DeficiencyC0086649
- Acetyl-CoA alpha-glucosaminide acetyltransferase deficiencyC0086649
- Acetyl-CoA: heparan-alpha-D-glucosaminide N-acetyltransferase deficiencyC0086649
- Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase DeficienciesC0086649
- Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase DeficiencyC0086649
- Deficiencies, Acetyl-CoA:alpha-Glucosaminide N-AcetyltransferaseC0086649
- Deficiency, Acetyl-CoA:alpha-Glucosaminide N-AcetyltransferaseC0086649
- Heparan-alpha-glucosaminide acetyltransferase deficiencyC0086649
- MPS 3 CC0086649
- MPS III CC0086649
- MPS III-C - Mucopolysaccharidosis III-CC0086649
- MPS IIICC0086649
- MPS3CC0086649
- MPSIIIC - Mucopolysaccharidosis type IIICC0086649
- MUCOPOLYSACCHARIDOSIS, TYPE IIICC0086649
- Mucopolysaccharidosis III-CC0086649
- Mucopolysaccharidosis III-C (disorder)C0086649
- Mucopolysaccharidosis Type 3 CC0086649
- Mucopolysaccharidosis Type IIICC0086649
- Mucopolysaccharidosis Type IIICsC0086649
- Mucopolysaccharidosis, MPS-III-CC0086649
- N-Acetyl transferase deficiencyC0086649
- N-Acetyltransferase Deficiencies, Acetyl-CoA:alpha-GlucosaminideC0086649
- N-Acetyltransferase Deficiency, Acetyl-CoA:alpha-GlucosaminideC0086649
- SANFILIPPO SYNDROME CC0086649
- Sanfilippo CC0086649
- Sanfilippo C syndromeC0086649
- Sanfilippo Syndrome CC0086649
- Sanfilippo syndrome CC0086649
- Sanfilippo syndrome, type CC0086649
- Alpha-N-acetylglucosaminidase deficiencyC0086648
- Deficiencies, N-Acetyl-alpha-D-GlucosaminidaseC0086648
- Deficiencies, NAGLUC0086648
- Deficiency, N-Acetyl-alpha-D-GlucosaminidaseC0086648
- Deficiency, NAGLUC0086648
- MPS 3 BC0086648
- MPS III BC0086648
- MPS III-B - Mucopolysaccharidosis III-BC0086648
- MPS IIIBC0086648
- MPS3BC0086648
- MPSIIIB - Mucopolysaccharidosis type IIIBC0086648
- MUCOPOLYSACCHARIDOSIS, TYPE IIIBC0086648
- Mucopolysaccharidosis III-BC0086648
- Mucopolysaccharidosis III-B (disorder)C0086648
- Mucopolysaccharidosis Type 3 BC0086648
- Mucopolysaccharidosis Type IIIBC0086648
- Mucopolysaccharidosis Type IIIBsC0086648
- Mucopolysaccharidosis, MPS-III-BC0086648
- N Acetyl alpha D Glucosaminidase DeficiencyC0086648
- N-ACETYL-ALPHA-D-GLUCOSAMINIDASE DEFICIENCYC0086648
- N-Acetyl-alpha-D-Glucosaminidase DeficienciesC0086648
- N-Acetyl-alpha-D-Glucosaminidase DeficiencyC0086648
- N-Acetyl-alpha-D-glucosaminidase deficiencyC0086648
- NAGLU DEFICIENCYC0086648
- NAGLU DeficienciesC0086648
- NAGLU DeficiencyC0086648
- SANFILIPPO SYNDROME BC0086648
- Sanfilippo BC0086648
- Sanfilippo B syndromeC0086648
- Sanfilippo Syndrome BC0086648
- Sanfilippo syndrome BC0086648
- Sanfilippo syndrome, type BC0086648
- alpha-N-acetylglucosaminidase deficiencyC0086648
- Deficiencies, N-Acetylglucosamine-6-SulfataseC0086650
- Deficiencies, N-Acetylglucosamine-6-Sulfate SulfataseC0086650
- Deficiency of N-acetylglucosamine-6-sulfataseC0086650
- Deficiency of N-acetylglucosamine-6-sulphataseC0086650
- Deficiency, N-Acetylglucosamine-6-SulfataseC0086650
- Deficiency, N-Acetylglucosamine-6-Sulfate SulfataseC0086650
- MPS 3 DC0086650
- MPS III DC0086650
- MPS III-D - Mucopolysaccharidosis III-DC0086650
- MPS IIIDC0086650
- MPS IIIDsC0086650
- MPS3DC0086650
- MPSIIID - Mucopolysaccharidosis type IIIDC0086650
- MUCOPOLYSACCHARIDOSIS, TYPE IIIDC0086650
- Mucopolysaccharidosis III-DC0086650
- Mucopolysaccharidosis III-D (disorder)C0086650
- Mucopolysaccharidosis Type 3 DC0086650
- Mucopolysaccharidosis Type IIIDC0086650
- Mucopolysaccharidosis Type IIIDsC0086650
- Mucopolysaccharidosis type IIIDC0086650
- Mucopolysaccharidosis, MPS-III-DC0086650
- N Acetylglucosamine 6 Sulfatase DeficiencyC0086650
- N Acetylglucosamine 6 Sulfate Sulfatase DeficiencyC0086650
- N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCYC0086650
- N-Acetylglucosamine-6-Sulfatase DeficienciesC0086650
- N-Acetylglucosamine-6-Sulfatase DeficiencyC0086650
- N-Acetylglucosamine-6-Sulfate Sulfatase DeficienciesC0086650
- N-Acetylglucosamine-6-Sulfate Sulfatase DeficiencyC0086650
- N-acetylglucosamine-6-sulfatase deficiencyC0086650
- N-acetylglucosamine-6-sulfate sulfatase deficiencyC0086650
- N-acetylglucosamine-6-sulphatase deficiencyC0086650
- SANFILIPPO SYNDROME DC0086650
- Sanfilippo DC0086650
- Sanfilippo D syndromeC0086650
- Sanfilippo Syndrome DC0086650
- Sanfilippo syndrome DC0086650
- Sanfilippo syndrome, type DC0086650
- Sulfatase Deficiencies, N-Acetylglucosamine-6-SulfateC0086650
- Sulfatase Deficiency, N-Acetylglucosamine-6-SulfateC0086650
- Deficiencies, SulfamidaseC0086647
- Deficiency, SulfamidaseC0086647
- HEPARAN SULFATE SULFATASE DEFICIENCYC0086647
- Heparan Sulfate Sulfatase DeficiencyC0086647
- Heparan sulfamidase deficiencyC0086647
- Heparan sulfate sulfatase deficiencyC0086647
- Heparan sulphamidase deficiencyC0086647
- Heparan sulphate sulphatase deficiencyC0086647
- Heparan-N-sulfatase deficiencyC0086647
- Heparan-N-sulphatase deficiencyC0086647
- MPS 3 AC0086647
- MPS III AC0086647
- MPS III-A - Mucopolysaccharidosis III-AC0086647
- MPS IIIAC0086647
- MPS3AC0086647
- MPSIIIA - Mucopolysaccharidosis type IIIAC0086647
- MUCOPOLYSACCHARIDOSIS, TYPE IIIAC0086647
- Mucopolysaccharidosis III-AC0086647
- Mucopolysaccharidosis III-A (disorder)C0086647
- Mucopolysaccharidosis Type 3 AC0086647
- Mucopolysaccharidosis Type 3 A Sanfilippo SyndromeC0086647
- Mucopolysaccharidosis Type IIIAC0086647
- Mucopolysaccharidosis Type IIIAsC0086647
- Mucopolysaccharidosis type IIIAC0086647
- Mucopolysaccharidosis, MPS-III-AC0086647
- N-sulfoglucosamine sulfohydrolase deficiencyC0086647
- N-sulphoglucosamine sulphohydrolase deficiencyC0086647
- SANFILIPPO SYNDROME AC0086647
- SULFAMIDASE DEFICIENCYC0086647
- Sanfilippo AC0086647
- Sanfilippo A syndromeC0086647
- Sanfilippo Syndrome AC0086647
- Sanfilippo syndrome AC0086647
- Sanfilippo syndrome, type AC0086647
- Sulfamidase DeficienciesC0086647
- Sulfamidase DeficiencyC0086647
- mp iiiC0086647
- mps iiiC0086647
- sanfilippo syndrome type aC0086647
- Mucopolysaccharidosis, type III (A) (B) (C) (D)C2874281
- Sanfilippo mucopolysaccharidosesC2874282
Frequently Asked Questions
What is the ICD-10 code for sanfilippo mucopolysaccharidoses?
The ICD-10-CM code for sanfilippo mucopolysaccharidoses is E76.22. The full clinical description is "Sanfilippo mucopolysaccharidoses". E76.22 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E76.22 mean?
ICD-10-CM code E76.22 represents "Sanfilippo mucopolysaccharidoses". 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 E76.22 a billable code?
Yes, E76.22 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E76.22 in?
E76.22 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E76.22?
E76.22 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 E76.22 map to?
E76.22 maps to 5 SNOMED CT concepts: 75238000, 59990008, 15892005, 41572006, 88393000. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E76.22?
E76.22 is linked to 6 UMLS Concept Unique Identifiers: C0086649, C0086648, C0086650, C0086647, C2874281, and 1 more. 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.