E76.219
BillableMorquio mucopolysaccharidoses, unspecified
Morquio mucopolysaccharidoses, unspecified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Morquio syndrome
- Mucopolysaccharidosis, type IV
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
- Congenital osteodystrophy5731000119108
UMLS
- Atypical chondrodystrophyC0026707
- Brailsford-Morquio syndromeC0026707
- Chondro-osteodystrophyC0026707
- Chondrodystrophia tardaC0026707
- Disease, MorquioC0026707
- Disease, Morquio'sC0026707
- Eccentro OsteochondrodysplasiaC0026707
- Eccentro-OsteochondrodysplasiaC0026707
- Eccentro-OsteochondrodysplasiasC0026707
- EccentroosteochondrodysplasiaC0026707
- EccentroosteochondrodysplasiasC0026707
- Familial osseous dystrophyC0026707
- Familial osteochondrodystrophyC0026707
- Hereditary enchondral dysostosisC0026707
- IV, Mucopolysaccharidosis TypeC0026707
- IVs, Mucopolysaccharidosis TypeC0026707
- Keratan sulfaturiaC0026707
- Keratan sulphaturiaC0026707
- MORQUIO DISC0026707
- MORQUIOS DISC0026707
- MPS 4C0026707
- MPS IVC0026707
- Morquio DiseaseC0026707
- Morquio SyndromeC0026707
- Morquio SyndromesC0026707
- Morquio diseaseC0026707
- Morquio syndromeC0026707
- Morquio syndrome (disorder)C0026707
- Morquio's DiseaseC0026707
- Morquio's SyndromeC0026707
- Morquio's diseaseC0026707
- Morquio's syndromeC0026707
- Morquio-Brailsford diseaseC0026707
- Morquio-Suarez syndromeC0026707
- Morquio-Ullrich diseaseC0026707
- Morquios DiseaseC0026707
- Morquios SyndromeC0026707
- Mucopolysaccharidosis (MPS) IV (A, B)C0026707
- Mucopolysaccharidosis 4C0026707
- Mucopolysaccharidosis IVC0026707
- Mucopolysaccharidosis Type IVC0026707
- Mucopolysaccharidosis Type IVsC0026707
- Mucopolysaccharidosis type IVC0026707
- Mucopolysaccharidosis, MPS-IVC0026707
- Mucopolysaccharidosis, type IVC0026707
- Osteochondrodystrophia deformansC0026707
- OsteochondrodystrophyC0026707
- Syndrome, MorquioC0026707
- Syndrome, Morquio'sC0026707
- Syndromes, MorquioC0026707
- Type IV, MucopolysaccharidosisC0026707
- Type IVs, MucopolysaccharidosisC0026707
- chondroosteodystrophyC0026707
- eccentroosteochondrodysplasiaC0026707
- morquio diseaseC0026707
- morquio syndromeC0026707
- morquio's diseaseC0026707
- morquio's syndromeC0026707
- morquios syndromeC0026707
- mucopolysaccharidosis type IVC0026707
- osteochondrodysplasiaC0026707
- osteochondrodystrophyC0026707
- spondylo-epiphyseal dysplasiaC0026707
- syndrome morquio'sC0026707
- Morquio mucopolysaccharidosesC2874280
- Morquio mucopolysaccharidoses, unspecifiedC2874280
Frequently Asked Questions
What is the ICD-10 code for morquio mucopolysaccharidoses, unspecified?
The ICD-10-CM code for morquio mucopolysaccharidoses, unspecified is E76.219. The full clinical description is "Morquio mucopolysaccharidoses, unspecified". E76.219 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E76.219 mean?
ICD-10-CM code E76.219 represents "Morquio mucopolysaccharidoses, unspecified". 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 E76.219 a billable code?
Yes, E76.219 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E76.219 in?
E76.219 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E76.219?
E76.219 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 E76.219 map to?
E76.219 maps to 2 SNOMED CT concepts: 378007, 5731000119108. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E76.219?
E76.219 is linked to 2 UMLS Concept Unique Identifiers: C0026707, C2874280. 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.