results found in ( seconds)
We are looking for ways to improve. If you have an suggestion for how ICD.Codes could be better, submit your idea!

ICD-10-CM Code E75.2
Other sphingolipidosis

Non-Billable Code
Non-Billable means the code is not sufficient justification for admission to an acute care hospital when used a principal diagnosis. Use a child code to capture more detail.
| ICD-10 from 2011 - 2016

ICD Code E75.2 is a non-billable code. To code a diagnosis of this type, you must use one of the six child codes of E75.2 that describes the diagnosis 'other sphingolipidosis' in more detail.

The ICD code E752 is used to code Multiple sulfatase deficiency

Multiple sulfatase deficiency (also known as "Austin disease," and "Mucosulfatidosis") is a very rare autosomal recessive:561 lysosomal storage disease caused by a deficiency in multiple sulfatase enzymes, or in formylglycine-generating enzyme, which activates sulfatases.:502 It is similar to mucopolysaccharidosis.

Specialty: Endocrinology
MeSH Codes: D052517, D055577, D009542, D017825, D020371, D052556, D009542, D007965
ICD 9 Codes: , 272.8, 272.7, 330.0, 330.0, 272.7, 272.7, 330.0
Source: Wikipedia

Coding Notes for E75.2 Info for medical coders on how to properly use this ICD-10 code

Code Type-1 Excludes:
Type-1 Excludes
Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here."
Adrenoleukodystrophy [Addison-Schilder] - instead, use code E71.528

Related Concepts SNOMET-CT

  • Megalencephalic leukoencephalopathy with subcortical cysts (disorder)
  • Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (disorder)

Parent Code: E75 - Disorders of sphingolipid metabolism and other lipid storage disorders

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/E752