E76.210
BillableMorquio A mucopolysaccharidoses
Morquio A mucopolysaccharidoses
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Classic Morquio syndrome
- Morquio syndrome A
- Mucopolysaccharidosis, type IVA
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
- Atypical chondrodystrophy378007
- Brailsford-Morquio syndrome378007
- Chondro-osteodystrophy378007
- Chondrodystrophia tarda378007
- Familial osseous dystrophy378007
- Familial osteochondrodystrophy378007
- Hereditary enchondral dysostosis378007
- Keratan sulfaturia378007
- Keratan sulphaturia378007
- Morquio disease378007
- Morquio syndrome378007
- Morquio-Brailsford disease378007
- Morquio-Suarez syndrome378007
- Morquio-Ullrich disease378007
- Mucopolysaccharidosis type IV378007
- Mucopolysaccharidosis, MPS-IV378007
- Osteochondrodystrophia deformans378007
- Osteochondrodystrophy378007
- Galactosamine-6-sulfatase deficiency7259005
- Galactosamine-6-sulphatase deficiency7259005
- Galactose-6-sulfatase deficiency7259005
- Galactose-6-sulphatase deficiency7259005
- MPS IV-A-Mucopolysaccharidosis IV-A7259005
- Morquio A syndrome7259005
- Morquio syndrome A7259005
- Morquio's syndrome, classic form7259005
- Mucopolysaccharidosis IV-A7259005
- Mucopolysaccharidosis, MPS-IV-A7259005
- N-acetylgalactosamine-6-sulfatase deficiency7259005
- N-acetylgalactosamine-6-sulphatase deficiency7259005
- Congenital osteodystrophy5731000119108
UMLS
- mps ivC0086651
- Deficiencies, Galactosamine-6-SulfataseC0086651
- Deficiency of N-acetylgalactosamine-6-sulfataseC0086651
- Deficiency of N-acetylgalactosamine-6-sulfatase (finding)C0086651
- Deficiency of N-acetylgalactosamine-6-sulphataseC0086651
- Deficiency of chondroitinaseC0086651
- Deficiency of chondroitinsulfataseC0086651
- Deficiency of chondroitinsulphataseC0086651
- Deficiency of galactose-6-sulfate sulfataseC0086651
- Deficiency of galactose-6-sulphate sulphataseC0086651
- Deficiency, Galactosamine-6-SulfataseC0086651
- Disease, Morquio AC0086651
- GALACTOSAMINE-6-SULFATASE DEFICIENCYC0086651
- GALNS DEFICIENCYC0086651
- Galactosamine 6 Sulfatase DeficiencyC0086651
- Galactosamine-6-Sulfatase DeficienciesC0086651
- Galactosamine-6-Sulfatase DeficiencyC0086651
- Galactosamine-6-sulfatase deficiencyC0086651
- Galactosamine-6-sulphatase deficiencyC0086651
- Galactose-6-sulfatase deficiencyC0086651
- Galactose-6-sulphatase deficiencyC0086651
- MORQUIO A DISEASEC0086651
- MORQUIO SYNDROME AC0086651
- MPS IV AC0086651
- MPS IV-A-Mucopolysaccharidosis IV-AC0086651
- MPS IVAC0086651
- MPS4AC0086651
- MUCOPOLYSACCHARIDOSIS, TYPE IVAC0086651
- Morquio A DiseaseC0086651
- Morquio A syndromeC0086651
- Morquio Syndrome AC0086651
- Morquio syndrome AC0086651
- Morquio's syndrome, classic formC0086651
- Mucopolysaccharidosis IV-AC0086651
- Mucopolysaccharidosis IV-A (disorder)C0086651
- Mucopolysaccharidosis Type IV AC0086651
- Mucopolysaccharidosis Type IVAC0086651
- Mucopolysaccharidosis, MPS-IV-AC0086651
- Mucopolysaccharidosis, type IVAC0086651
- N-acetylgalactosamine-6-sulfatase deficiencyC0086651
- N-acetylgalactosamine-6-sulphatase deficiencyC0086651
- Syndrome A, MorquioC0086651
- Classic Morquio syndromeC2874276
- Morquio A mucopolysaccharidosesC2874277
Frequently Asked Questions
What is the ICD-10 code for morquio a mucopolysaccharidoses?
The ICD-10-CM code for morquio a mucopolysaccharidoses is E76.210. The full clinical description is "Morquio A mucopolysaccharidoses". E76.210 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E76.210 mean?
ICD-10-CM code E76.210 represents "Morquio A 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 E76.210 a billable code?
Yes, E76.210 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E76.210 in?
E76.210 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E76.210?
E76.210 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 E76.210 map to?
E76.210 maps to 3 SNOMED CT concepts: 378007, 5731000119108, 7259005. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E76.210?
E76.210 is linked to 3 UMLS Concept Unique Identifiers: C0086651, C2874276, C2874277. 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.