AutoICD API

E75.29

Billable

Other sphingolipidosis

Other sphingolipidosis

Status

Billable / Specific

Block

E70-E88

Parent Code

E75.2

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Farber's syndrome
  • Sulfatide lipidosis

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(8)
E75.21

Fabry (-Anderson) disease

BillableE75.22

Gaucher disease

BillableE75.23

Krabbe disease

BillableE75.24

Niemann-Pick disease

E75.25

Metachromatic leukodystrophy

BillableE75.26

Sulfatase deficiency

BillableE75.27

Pelizaeus-Merzbacher disease

BillableE75.28

Canavan disease

Billable
Also Known As / Clinical Terms(404)

SNOMED CT

UMLS

Clinical Terms

  • mld
  • Multiple sulphatase deficiency
  • Ovarioleucodystrophy
  • Myelinosis centralis diffusa
  • 4H leucodystrophy
  • Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency
  • Steryl-sulphate sulphohydrolase deficiency
  • TUBB4A (tubulin beta 4A class IVa) related leukodystrophy
  • Arylsulphatase C deficiency
  • PLP1 null syndrome
  • Premature ovarian failure
  • TUBB4A-related leukodystrophy
  • Waardenburg syndrome
  • Spongy degeneration of white matter
  • Deficiency of arylsulfatase
  • RNA polymerase III-related leukodystrophy
  • Deficiency of galactose-6-sulphate sulphatase
  • Adult onset autosomal dominant leucodystrophy
  • Leucodystrophy due to alkaline ceramidase 3 deficiency
  • Leukoencephalopathy with vanishing white matter
  • Cerebral sclerosis, diffuse, metachromatic form
  • Deficiency of chondroitinase
  • Encephalopathy due to prosaposin deficiency
  • Deficiency of 6-sulphatase
  • Combined saposin deficiency
  • Deficiency of galactose-6-sulfate sulfatase
  • VPS11-related autosomal recessive hypomyelinating leucoencephalopathy
  • TUBB4A-related hypomyelinating leukodystrophy
  • Vanishing white matter disease
  • Sulfatide Lipidosis
  • Pelizaeus-Merzbacher disease, classic form
  • Deficiency of placental endocrine function
  • Deficiency of N-acetylgalactosamine-6-sulphatase
  • Pelizaeus-Merzbacher disease, connatal variant
  • H-ABC - hypomyelination, atrophy of basal ganglia and cerebellum
  • Deficiency of chondroitinsulfatase
  • Sex-linked ichthyosis
  • Deficiency of steryl-sulphatase
  • Placental steroidal sulfatase deficiency
  • Type V atypical Pelizaeus-Merzbacher disease
  • Type VI Cockayne Pelizaeus-Merzbacher disease
  • Familial infantile diffuse brain sclerosis
  • SPAX8 - spastic ataxia 8
  • Childhood ataxia with diffuse central nervous system hypomyelination
  • Hereditary cerebellar atrophy
  • Aspartoacylase deficiency
  • Autosomal recessive hypomyelinating leucodystrophy, progressive spastic ataxia
  • C11ORF73-related autosomal recessive hypomyelinating leucoencephalopathy
  • Arylsulfatase C deficiency
  • Pelizaeus Merzbacher like disease due to HSPD1 mutation
  • Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leucodystrophy
  • Dementia due to leukodystrophy
  • Neuroaxonal dystrophy
  • Globoid cell leukodystrophy, early onset
  • Ribonucleic acid polymerase III-related leukodystrophy
  • C11ORF73-related autosomal recessive hypomyelinating leukodystrophy
  • ARYLSULFATASE A DEFIC DIS
  • MLD - Metachromatic leucodystrophy
  • metachromatic leukoencephalopathy
  • RNA polymerase III-related leucodystrophy
  • RARS-related autosomal recessive hypomyelinating leukodystrophy
  • Placental sulfatase deficiency
  • Hypomyelination with atrophy of basal ganglia and cerebellum syndrome
  • Adult onset autosomal dominant leukodystrophy
  • VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy
  • Odontoleukodystrophy
  • VPS11-related autosomal recessive hypomyelinating leukodystrophy
  • CACH (childhood ataxia with diffuse central nervous system hypomyelination) syndrome
  • POLR-related leucodystrophy
  • Pelizaeus Merzbacher like disease due to AIMP1 mutation
  • Deficiency of 6-sulfatase
  • Ovarioleukodystrophy
  • Neurologic Waardenburg Shah syndrome
  • Canavan's disease
  • Pelizaeus-Merzbacher disease null syndrome
  • PMLD - Pelizaeus Merzbacher like disease
  • Deficiency of arylsulphatase
  • POLR-related leukodystrophy
  • Sulphatide lipidosis
  • Cerebroside sulphatase deficiency disease
  • van Bogaert-Nijssen disease
  • Muscle eye brain disease with bilateral multicystic leucodystrophy
  • Arylsulfatase A Deficiency Disease
  • Deficiency of cerebroside-sulphatase
  • Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
  • Leukodystrophy
  • Farber's syndrome
  • Type I classic Pelizaeus-Merzbacher disease
  • Hypomyelinating leukodystrophy due to HIKESHI deficiency
  • Juvenile sulphatidosis, Austin type
  • VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leucodystrophy
  • VPS11-related autosomal recessive hypomyelinating leucodystrophy
  • Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy
  • Metachromatic Leukoencephalopathies
  • Juvenile sulfatidosis, Austin type
  • Spastic tetraplegia
  • Muscle eye brain disease with bilateral multicystic leukodystrophy
  • Disorder of placental endocrine function
  • Leukodystrophy, Metachromatic
  • Metachromatic leukodystrophy
  • Pelizaeus Merzbacher like disease due to GJC2 mutation
  • Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy
  • POF - Premature ovarian failure
  • CEREBROSIDE SULPHATASE DEFIC DIS
  • Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy
  • Tubulin beta 4A class IVa related leukodystrophy
  • sulfatide lipoidosis
  • X-linked placental steryl-sulfatase deficiency
  • Hypomyelinating leucodystrophy with atrophy of basal ganglia and cerebellum
  • Leucoencephalopathy with vanishing white matter
  • Combined malformation of central nervous system and skeletal muscle
  • Canavan-van-Bogaert-Bertrand disease
  • Deficiency of cerebroside-sulfatase
  • Disorder involving deficiency of steryl-sulfatase (EC 3.1.6.2)
  • Leukodystrophy due to alkaline ceramidase 3 deficiency
  • CEREBROSIDE SULFATASE DEFICIENCY
  • Waardenburg's syndrome
  • Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
  • Sudanophilic leukodystrophy
  • Mucosulphatidosis
  • X-linked placental steryl-sulphatase deficiency
  • Multiple sulfatase deficiency
  • Metachromatic Leukodystrophies
  • Pelizaeus-Merzbacher disease in female carrier
  • X-linked ichthyosis with steryl-sulphatase deficiency
  • Metachromatic leukoencephaly
  • NK6 homeobox 2-related autosomal recessive hypomyelinating leucodystrophy
  • Pelizaeus Merzbacher like disease due to SLC16A2 mutation
  • Deficiency of chondroitinsulphatase
  • Hypomyelinating leucodystrophy due to HIKESHI deficiency
  • Ribonucleic acid polymerase III-related leucodystrophy
  • VPS11-related autosomal recessive hypomyelinating leukoencephalopathy
  • Placental steroidal sulphatase deficiency
  • Juvenile sulphatidosis Austin type
  • Mucosulfatidosis
  • Combined prosaposin deficiency
  • X-linked ichthyosis with steryl-sulfatase deficiency
  • C11ORF73-related autosomal recessive hypomyelinating leucodystrophy
  • Deficiency of placental function
  • metachromatic leucodystrophy
  • leukodystrophy metachromatic
  • Leukoencephalopathy, Metachromatic
  • Spongy degeneration of central nervous system
  • Null syndrome
  • Type II congenital Pelizaeus-Merzbacher disease
  • Neuroaxonal leucodystrophy
  • Leucodystrophy with oligodontia
  • Steroid sulfatase deficiency
  • Neuroaxonal leukodystrophy
  • Scholz cerebral sclerosis
  • Deficiency of steryl-sulfatase
  • Dementia due to leucodystrophy
  • 4H leukodystrophy
  • RARS-related autosomal recessive hypomyelinating leucodystrophy
  • Spongiform leucodystrophy
  • Familial progressive cerebral sclerosis
  • NKX6-2-related autosomal recessive hypomyelinating leukodystrophy
  • Autosomal recessive hypomyelinating leukodystrophy, progressive spastic ataxia
  • Dystonia due to Pelizaeus-Merzbacher disease
  • Juvenile sulfatidosis Austin type
  • Steroid sulphatase deficiency
  • Leucodystrophy
  • Deficiency of N-acetylgalactosamine-6-sulfatase
  • PCWH - peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
  • Metachromatic leucodystrophy (disorder)
  • Galactosylceramide lipidosis
  • Alkaline ceramidase 3 deficiency
  • Canavan-van Bogaert-Bertrand disease
  • Spastic quadriplegia
  • ACER3-related early childhood-onset progressive leukodystrophy
  • Type III transitional Pelizaeus-Merzbacher disease
  • Leukoencephalopathies, Metachromatic
  • Leukodystrophy with oligodontia
  • NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy
  • Pelizaeus Merzbacher like disease
  • Diffuse globoid body sclerosis
  • NKX6-2-related autosomal recessive hypomyelinating leucodystrophy
  • Placental sulfatase deficiency (X-linked steryl-sulfatase deficiency) in a female
  • Dentoleukoencephalopathy
  • Spongy degeneration of white matter in infancy
  • X-linked ichthyosis
  • Pelizaeus-Merzbacher disease
  • Leukodystrophies, Metachromatic
  • Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosis
  • Lipidosis, Sulfatide
  • C11ORF73-related autosomal recessive hypomyelinating leukoencephalopathy
  • ACER3-related early childhood-onset progressive leucodystrophy
  • Placental sulphatase deficiency
  • Steryl-sulfate sulfohydrolase deficiency
  • Type IV adult Pelizaeus-Merzbacher disease
Frequently Asked Questions
What is the ICD-10 code for other sphingolipidosis?

The ICD-10-CM code for other sphingolipidosis is E75.29. The full clinical description is "Other sphingolipidosis". E75.29 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E75.29 mean?

ICD-10-CM code E75.29 represents “Other sphingolipidosis”. 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 E75.29 a billable code?

Yes, E75.29 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E75.29 in?

E75.29 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E75.29?

E75.29 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 6 more.

What SNOMED CT codes does E75.29 map to?

E75.29 maps to 54 SNOMED CT concepts: 1208933000, 1237515001, 448054001, 1220600004, 3642008, and 49 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E75.29?

E75.29 is linked to 3 UMLS Concept Unique Identifiers: C0023522, C2874274, C0348489. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E75.29 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other sphingolipidosis 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 E75.29?

There is no direct ICD-11 mapping available for E75.29 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.

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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.