The ICD-10 code for Mucopolysaccharidosis, type II is E76.1.2026 ICD-10-CM Diagnosis Code E76.1 – Mucopolysaccharidosis, type II Related ICD-10 Codes Parent code: E76 – Disorders of glycosaminoglycan metabolism Other codes in same category: E76.0 – Mucopolysaccharidosis, type I, E76.01 – Hurler's syndrome, E76.02 – Hurler-Scheie syndrome, E76.03 – Scheie's syndrome, E76.2 – Other mucopolysaccharidoses, E76.21…

The ICD-10 code for Scheie’s syndrome is E76.03.2026 ICD-10-CM Diagnosis Code E76.03 – Scheie’s syndrome Related ICD-10 Codes Parent code: E76 – Disorders of glycosaminoglycan metabolism Other codes in same category: E76.0 – Mucopolysaccharidosis, type I, E76.01 – Hurler's syndrome, E76.02 – Hurler-Scheie syndrome, E76.1 – Mucopolysaccharidosis, type II, E76.2 – Other mucopolysaccharidoses, E76.21 –…

The ICD-10 code for Hurler-Scheie syndrome is E76.02.2026 ICD-10-CM Diagnosis Code E76.02 – Hurler-Scheie syndrome Related ICD-10 Codes Parent code: E76 – Disorders of glycosaminoglycan metabolism Other codes in same category: E76.0 – Mucopolysaccharidosis, type I, E76.01 – Hurler's syndrome, E76.03 – Scheie's syndrome, E76.1 – Mucopolysaccharidosis, type II, E76.2 – Other mucopolysaccharidoses, E76.21 –…

The ICD-10 code for Hurler’s syndrome is E76.01.2026 ICD-10-CM Diagnosis Code E76.01 – Hurler’s syndrome Related ICD-10 Codes Parent code: E76 – Disorders of glycosaminoglycan metabolism Other codes in same category: E76.0 – Mucopolysaccharidosis, type I, E76.02 – Hurler-Scheie syndrome, E76.03 – Scheie's syndrome, E76.1 – Mucopolysaccharidosis, type II, E76.2 – Other mucopolysaccharidoses, E76.21 –…

The ICD-10 code for Mucopolysaccharidosis, type I is E76.0.2026 ICD-10-CM Diagnosis Code E76.0 – Mucopolysaccharidosis, type I Related ICD-10 Codes Parent code: E76 – Disorders of glycosaminoglycan metabolism Other codes in same category: E76.01 – Hurler's syndrome, E76.02 – Hurler-Scheie syndrome, E76.03 – Scheie's syndrome, E76.1 – Mucopolysaccharidosis, type II, E76.2 – Other mucopolysaccharidoses, E76.21…

The ICD-10 code for Disorders of glycosaminoglycan metabolism is E76.2026 ICD-10-CM Diagnosis Code E76 – Disorders of glycosaminoglycan metabolism Related ICD-10 Codes More specific subcodes: E76.0 – Mucopolysaccharidosis, type I, E76.01 – Hurler's syndrome, E76.02 – Hurler-Scheie syndrome, E76.03 – Scheie's syndrome, E76.1 – Mucopolysaccharidosis, type II, E76.2 – Other mucopolysaccharidoses, E76.21 – Morquio mucopolysaccharidoses,…

The ICD-10 code for Lipid storage disorder, unspecified is E75.6.2026 ICD-10-CM Diagnosis Code E75.6 – Lipid storage disorder, unspecified Related ICD-10 Codes Parent code: E75 – Disorders of sphingolipid metabolism and other lipid storage disorders Other codes in same category: E75.0 – GM2 gangliosidosis, E75.00 – GM2 gangliosidosis, unspecified, E75.01 – Sandhoff disease, E75.02 –…

The ICD-10 code for Other lipid storage disorders is E75.5.2026 ICD-10-CM Diagnosis Code E75.5 – Other lipid storage disorders Related ICD-10 Codes Parent code: E75 – Disorders of sphingolipid metabolism and other lipid storage disorders Other codes in same category: E75.0 – GM2 gangliosidosis, E75.00 – GM2 gangliosidosis, unspecified, E75.01 – Sandhoff disease, E75.02 –…

The ICD-10 code for Neuronal ceroid lipofuscinosis is E75.4.2026 ICD-10-CM Diagnosis Code E75.4 – Neuronal ceroid lipofuscinosis Related ICD-10 Codes Parent code: E75 – Disorders of sphingolipid metabolism and other lipid storage disorders Other codes in same category: E75.0 – GM2 gangliosidosis, E75.00 – GM2 gangliosidosis, unspecified, E75.01 – Sandhoff disease, E75.02 – Tay-Sachs disease,…

The ICD-10 code for Sphingolipidosis, unspecified is E75.3.2026 ICD-10-CM Diagnosis Code E75.3 – Sphingolipidosis, unspecified Related ICD-10 Codes Parent code: E75 – Disorders of sphingolipid metabolism and other lipid storage disorders Other codes in same category: E75.0 – GM2 gangliosidosis, E75.00 – GM2 gangliosidosis, unspecified, E75.01 – Sandhoff disease, E75.02 – Tay-Sachs disease, E75.09 –…