AutoICD API

E76.22

Billable

Sanfilippo mucopolysaccharidoses

Sanfilippo mucopolysaccharidoses

Status

Billable / Specific

Block

E70-E88

Parent Code

E76.2

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

Related Codes(2)
E76.21

Morquio mucopolysaccharidoses

E76.29

Other mucopolysaccharidoses

Billable
Also Known As / Clinical Terms(319)

SNOMED CT

UMLS

Clinical Terms

  • Sanfilippo syndrome
  • Sanfilippo Syndrome C
  • MPS III-A - Mucopolysaccharidosis III-A
  • SANFILIPPO SYNDROME A
  • N Acetylglucosamine 6 Sulfate Sulfatase Deficiency
  • Mucopolysaccharidosis Type IIIDs
  • Deficiencies, N-Acetylglucosamine-6-Sulfate Sulfatase
  • Sanfilippo C
  • Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiencies
  • MPS IIID
  • Alpha-N-acetylglucosaminidase deficiency
  • MPS III B
  • Sanfilippo syndrome, type C
  • Mucopolysaccharidosis type IIIA
  • Mucopolysaccharidosis Type 3 C
  • Mucopolysaccharidosis III-D
  • Deficiencies, N-Acetyl-alpha-D-Glucosaminidase
  • Mucopolysaccharidosis III-A
  • sanfilippo syndrome type a
  • NAGLU DEFICIENCY
  • N-Acetyl-alpha-D-Glucosaminidase Deficiencies
  • N-Acetyltransferase Deficiency, Acetyl-CoA:alpha-Glucosaminide
  • MPS III C
  • MPSIIIB - Mucopolysaccharidosis type IIIB
  • Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiency
  • MPS IIIC
  • Sanfilippo disease
  • SANFILIPPO SYNDROME D
  • Sulfamidase Deficiency
  • Mucopolysaccharidosis, MPS-III-D
  • Deficiency, Sulfamidase
  • Acetyl-CoA: heparan-alpha-D-glucosaminide N-acetyltransferase deficiency
  • N-Acetyl-alpha-D-glucosaminidase deficiency
  • Deficiencies, Sulfamidase
  • Heparan Sulfate Sulfatase Deficiency
  • Mucopolysaccharidosis Type 3 A
  • Mucopolysaccharidosis Type IIIB
  • Deficiencies, N-Acetylglucosamine-6-Sulfatase
  • Mucopolysaccharidosis, MPS-III
  • MPS3C
  • Heparan-N-sulfatase deficiency
  • Mucopolysaccharidosis Type 3 A Sanfilippo Syndrome
  • MPS IIIDs
  • Mucopolysaccharidosis, MPS-III-B
  • N-Acetyltransferase Deficiencies, Acetyl-CoA:alpha-Glucosaminide
  • N-sulfoglucosamine sulfohydrolase deficiency
  • Deficiency, Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase
  • MPS III-D - Mucopolysaccharidosis III-D
  • N-acetylglucosamine-6-sulphatase deficiency
  • Deficiency, NAGLU
  • N-Acetylglucosamine-6-Sulfatase Deficiency
  • MPS 3 B
  • MUCOPOLYSACCHARIDOSIS, TYPE IIIB
  • Mucopolysaccharidosis III-B
  • Heparan-N-sulphatase deficiency
  • Sanfilippo C syndrome
  • Mucopolysaccharidosis Type IIIC
  • MPS 3 C
  • N Acetyl alpha D Glucosaminidase Deficiency
  • Heparan sulphamidase deficiency
  • Sanfilippo D syndrome
  • Deficiency of N-acetylglucosamine-6-sulfatase
  • MPSIIIC - Mucopolysaccharidosis type IIIC
  • Mucopolysaccharidosis type IIID
  • N Acetylglucosamine 6 Sulfatase Deficiency
  • N-Acetylglucosamine-6-Sulfate Sulfatase Deficiencies
  • NAGLU Deficiencies
  • Mucopolysaccharidosis Type IIIBs
  • Mucopolysaccharidosis Type 3 B
  • Sanfilippo B syndrome
  • MPS III D
  • MPS 3 A
  • Mucopolysaccharidosis Type 3 D
  • N-sulphoglucosamine sulphohydrolase deficiency
  • Mucopolysaccharidosis Type IIICs
  • Deficiency, N-Acetyl-alpha-D-Glucosaminidase
  • mp iii
  • Sanfilippo Syndrome B
  • MPSIIIA - Mucopolysaccharidosis type IIIA
  • Acetyl-CoA alpha-glucosaminide acetyltransferase deficiency
  • Mucopolysaccharidosis, MPS-III-A
  • Sanfilippo syndrome, type B
  • Mucopolysaccharidosis III-D (disorder)
  • N-Acetyl transferase deficiency
  • Mucopolysaccharidosis III-A (disorder)
  • MUCOPOLYSACCHARIDOSIS, TYPE IIIC
  • MPS3A
  • Deficiency of N-acetylglucosamine-6-sulphatase
  • Deficiency, N-Acetylglucosamine-6-Sulfate Sulfatase
  • Mucopolysaccharidosis, MPS-III-C
  • Sulfamidase Deficiencies
  • MUCOPOLYSACCHARIDOSIS, TYPE IIID
  • Mucopolysaccharidosis, type III (A) (B) (C) (D)
  • Sanfilippo B
  • Heparan sulfamidase deficiency
  • N-Acetylglucosamine-6-Sulfatase Deficiencies
  • MPS 3 D
  • N-Acetylglucosamine-6-Sulfate Sulfatase Deficiency
  • Sanfilippo D
  • MUCOPOLYSACCHARIDOSIS, TYPE IIIA
  • Sanfilippo A
  • Deficiencies, NAGLU
  • MPS IIIB
  • Mucopolysaccharidosis III-C
  • MPS III A
  • Mucopolysaccharidosis Type IIIAs
  • Sulfatase Deficiencies, N-Acetylglucosamine-6-Sulfate
  • MPS III-C - Mucopolysaccharidosis III-C
  • MPS III-B - Mucopolysaccharidosis III-B
  • Mucopolysaccharidosis III-C (disorder)
  • Sanfilippo syndrome, type A
  • Mucopolysaccharidosis type III
  • Sanfilippo syndrome, type D
  • Acetyl CoA:alpha Glucosaminide N Acetyltransferase Deficiency
  • Heparan sulphate sulphatase deficiency
  • Mucopolysaccharidosis III-B (disorder)
  • Sulfatase Deficiency, N-Acetylglucosamine-6-Sulfate
  • Heparan-alpha-glucosaminide acetyltransferase deficiency
  • Deficiencies, Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase
  • MPS3B
  • MPS IIIA
  • mps iii
  • MPS3D
  • Deficiency, N-Acetylglucosamine-6-Sulfatase
  • MPSIIID - Mucopolysaccharidosis type IIID
  • Sanfilippo A syndrome
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.

How does E76.22 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like sanfilippo mucopolysaccharidoses 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 E76.22?

There is no direct ICD-11 mapping available for E76.22 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try FreeView API Docs

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.