E75.29
BillableOther sphingolipidosis
Other sphingolipidosis
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)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- mucolipidosis, types I-III (E77.0-E77.1)
- Refsum's disease (G60.1)
- adrenoleukodystrophy [Addison-Schilder] (E71.528)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Arylsulfatase C deficiency3642008
- Arylsulphatase C deficiency3642008
- Deficiency of steryl-sulfatase3642008
- Deficiency of steryl-sulphatase3642008
- Disorder involving deficiency of steryl-sulfatase (EC 3.1.6.2)3642008
- Steryl-sulfate sulfohydrolase deficiency3642008
- Steryl-sulphate sulphohydrolase deficiency3642008
- Placental steroidal sulfatase deficiency3944006
- Placental steroidal sulphatase deficiency3944006
- Placental sulfatase deficiency3944006
- Placental sulfatase deficiency (X-linked steryl-sulfatase deficiency) in a female3944006
- Placental sulphatase deficiency3944006
- Steroid sulfatase deficiency3944006
- Steroid sulphatase deficiency3944006
- X-linked placental steryl-sulfatase deficiency3944006
- X-linked placental steryl-sulphatase deficiency3944006
- Waardenburg syndrome47434006
- Waardenburg's syndrome47434006
- Juvenile sulfatidosis Austin type54898003
- Juvenile sulfatidosis, Austin type54898003
- Juvenile sulphatidosis Austin type54898003
- Juvenile sulphatidosis, Austin type54898003
- Mucosulfatidosis54898003
- Mucosulphatidosis54898003
- Multiple sulfatase deficiency54898003
- Multiple sulphatase deficiency54898003
- Pelizaeus-Merzbacher disease, connatal variant59636002
- Type II congenital Pelizaeus-Merzbacher disease59636002
- Pelizaeus-Merzbacher disease64855000
- Sudanophilic leukodystrophy64855000
- Deficiency of cerebroside-sulfatase66521008
- Deficiency of cerebroside-sulphatase66521008
- Deficiency of placental function68635007
- Deficiency of placental endocrine function70137000
- Disorder of placental endocrine function70137000
- Sex-linked ichthyosis72523005
- X-linked ichthyosis72523005
- X-linked ichthyosis with steryl-sulfatase deficiency72523005
- X-linked ichthyosis with steryl-sulphatase deficiency72523005
- Aspartoacylase deficiency80544005
- Canavan's disease80544005
- Canavan-van Bogaert-Bertrand disease80544005
- Canavan-van-Bogaert-Bertrand disease80544005
- Spongiform leucodystrophy80544005
- Spongy degeneration of central nervous system80544005
- Spongy degeneration of white matter80544005
- Spongy degeneration of white matter in infancy80544005
- Pelizaeus-Merzbacher disease, classic form87607002
- Type I classic Pelizaeus-Merzbacher disease87607002
- Deficiency of N-acetylgalactosamine-6-sulfatase130197005
- Deficiency of N-acetylgalactosamine-6-sulphatase130197005
- Deficiency of chondroitinase130197005
- Deficiency of chondroitinsulfatase130197005
- Deficiency of chondroitinsulphatase130197005
- Deficiency of galactose-6-sulfate sulfatase130197005
- Deficiency of galactose-6-sulphate sulphatase130197005
- Diffuse globoid body sclerosis189979005
- Familial infantile diffuse brain sclerosis189979005
- Galactosylceramide lipidosis189979005
- Globoid cell leukodystrophy, early onset189979005
- Leucodystrophy192781003
- Leukodystrophy192781003
- Spastic quadriplegia192965001
- Spastic tetraplegia192965001
- Neuroaxonal dystrophy230365004
- Neuroaxonal leucodystrophy230367007
- Neuroaxonal leukodystrophy230367007
- Type III transitional Pelizaeus-Merzbacher disease230368002
- Type IV adult Pelizaeus-Merzbacher disease230369005
- Type V atypical Pelizaeus-Merzbacher disease230370006
- Type VI Cockayne Pelizaeus-Merzbacher disease230371005
- POF - Premature ovarian failure237788002
- Premature ovarian failure237788002
- Combined malformation of central nervous system and skeletal muscle277949001
- Deficiency of 6-sulfatase360834005
- Deficiency of 6-sulphatase360834005
- Deficiency of arylsulfatase360834005
- Deficiency of arylsulphatase360834005
- Familial progressive cerebral sclerosis396338004
- MLD - Metachromatic leucodystrophy396338004
- Metachromatic leucodystrophy396338004
- Metachromatic leukodystrophy396338004
- Metachromatic leukoencephaly396338004
- Sulfatide lipidosis396338004
- Sulphatide lipidosis396338004
- van Bogaert-Nijssen disease396338004
- CACH (childhood ataxia with diffuse central nervous system hypomyelination) syndrome447351004
- Childhood ataxia with diffuse central nervous system hypomyelination447351004
- Leucoencephalopathy with vanishing white matter447351004
- Leukoencephalopathy with vanishing white matter447351004
- Myelinosis centralis diffusa447351004
- Vanishing white matter disease447351004
- Adult onset autosomal dominant leucodystrophy448054001
- Adult onset autosomal dominant leukodystrophy448054001
- RNA polymerase III-related leucodystrophy712637001
- RNA polymerase III-related leukodystrophy712637001
- Ribonucleic acid polymerase III-related leucodystrophy712637001
- Ribonucleic acid polymerase III-related leukodystrophy712637001
- PMLD - Pelizaeus Merzbacher like disease717042001
- Pelizaeus Merzbacher like disease717042001
- Combined prosaposin deficiency720864008
- Combined saposin deficiency720864008
- Encephalopathy due to prosaposin deficiency720864008
- Dentoleukoencephalopathy722064003
- Leucodystrophy with oligodontia722064003
- Leukodystrophy with oligodontia722064003
- Odontoleukodystrophy722064003
- H-ABC - hypomyelination, atrophy of basal ganglia and cerebellum724283004
- Hypomyelinating leucodystrophy with atrophy of basal ganglia and cerebellum724283004
- Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum724283004
- Hypomyelination with atrophy of basal ganglia and cerebellum syndrome724283004
- Neurologic Waardenburg Shah syndrome765325002
- PCWH - peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease765325002
- Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease765325002
- TUBB4A (tubulin beta 4A class IVa) related leukodystrophy769065000
- TUBB4A-related hypomyelinating leukodystrophy769065000
- TUBB4A-related leukodystrophy769065000
- Tubulin beta 4A class IVa related leukodystrophy769065000
- Muscle eye brain disease with bilateral multicystic leucodystrophy785298001
- Muscle eye brain disease with bilateral multicystic leukodystrophy785298001
- Pelizaeus Merzbacher like disease due to HSPD1 mutation870284000
- Pelizaeus Merzbacher like disease due to SLC16A2 mutation870285004
- Pelizaeus Merzbacher like disease due to AIMP1 mutation870286003
- Pelizaeus Merzbacher like disease due to GJC2 mutation870287007
- Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency1003375005
- Null syndrome1003447007
- PLP1 null syndrome1003447007
- Pelizaeus-Merzbacher disease null syndrome1003447007
- Pelizaeus-Merzbacher disease in female carrier1003881009
- Ovarioleucodystrophy1156768008
- Ovarioleukodystrophy1156768008
- C11ORF73-related autosomal recessive hypomyelinating leucodystrophy1172595004
- C11ORF73-related autosomal recessive hypomyelinating leucoencephalopathy1172595004
- C11ORF73-related autosomal recessive hypomyelinating leukodystrophy1172595004
- C11ORF73-related autosomal recessive hypomyelinating leukoencephalopathy1172595004
- Hypomyelinating leucodystrophy due to HIKESHI deficiency1172595004
- Hypomyelinating leukodystrophy due to HIKESHI deficiency1172595004
- VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leucodystrophy1187249005
- VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy1187249005
- VPS11-related autosomal recessive hypomyelinating leucodystrophy1187249005
- VPS11-related autosomal recessive hypomyelinating leucoencephalopathy1187249005
- VPS11-related autosomal recessive hypomyelinating leukodystrophy1187249005
- VPS11-related autosomal recessive hypomyelinating leukoencephalopathy1187249005
- 4H leucodystrophy1208933000
- 4H leukodystrophy1208933000
- POLR-related leucodystrophy1208933000
- POLR-related leukodystrophy1208933000
- Autosomal recessive hypomyelinating leucodystrophy, progressive spastic ataxia1217379007
- Autosomal recessive hypomyelinating leukodystrophy, progressive spastic ataxia1217379007
- NK6 homeobox 2-related autosomal recessive hypomyelinating leucodystrophy1217379007
- NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy1217379007
- NKX6-2-related autosomal recessive hypomyelinating leucodystrophy1217379007
- NKX6-2-related autosomal recessive hypomyelinating leukodystrophy1217379007
- SPAX8 - spastic ataxia 81217379007
- Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy1220598005
- Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy1220598005
- Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leucodystrophy1220600004
- Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy1220600004
- RARS-related autosomal recessive hypomyelinating leucodystrophy1220600004
- RARS-related autosomal recessive hypomyelinating leukodystrophy1220600004
- ACER3-related early childhood-onset progressive leucodystrophy1237515001
- ACER3-related early childhood-onset progressive leukodystrophy1237515001
- Alkaline ceramidase 3 deficiency1237515001
- Leucodystrophy due to alkaline ceramidase 3 deficiency1237515001
- Leukodystrophy due to alkaline ceramidase 3 deficiency1237515001
- Dementia due to leucodystrophy1259494002
- Dementia due to leukodystrophy1259494002
- Dystonia due to Pelizaeus-Merzbacher disease1260363007
- Hereditary cerebellar atrophy431641000124107
UMLS
- ARYLSULFATASE A DEFIC DISC0023522
- Arylsulfatase A Deficiency DiseaseC0023522
- CEREBRAL SCLEROSIS, DIFFUSE, METACHROMATIC FORMC0023522
- CEREBROSIDE SULFATASE DEFICIENCYC0023522
- CEREBROSIDE SULPHATASE DEFIC DISC0023522
- Cerebral sclerosis, Diffuse, Metachromatic FormC0023522
- Cerebral sclerosis, diffuse, metachromatic formC0023522
- Cerebroside Sulphatase Deficiency DiseaseC0023522
- Cerebroside sulphatase deficiency diseaseC0023522
- Familial progressive cerebral sclerosisC0023522
- Leukodystrophies, MetachromaticC0023522
- Leukodystrophy, MetachromaticC0023522
- Leukoencephalopathies, MetachromaticC0023522
- Leukoencephalopathy, MetachromaticC0023522
- Lipidosis, SulfatideC0023522
- METACHROMATIC LEUKODYSTROPHYC0023522
- METACHROMATIC LEUKOENCEPHALOPATHYC0023522
- MLDC0023522
- MLD - Metachromatic leucodystrophyC0023522
- Metachromatic LeukodystrophiesC0023522
- Metachromatic LeukodystrophyC0023522
- Metachromatic LeukoencephalopathiesC0023522
- Metachromatic LeukoencephalopathyC0023522
- Metachromatic leucodystrophyC0023522
- Metachromatic leucodystrophy (disorder)C0023522
- Metachromatic leukodystrophyC0023522
- Metachromatic leukoencephalopathyC0023522
- Metachromatic leukoencephalyC0023522
- SULFATIDE LIPIDOSISC0023522
- Scholz cerebral sclerosisC0023522
- Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosisC0023522
- Sulfatide LipidosisC0023522
- Sulfatide lipidosisC0023522
- Sulphatide lipidosisC0023522
- leukodystrophy metachromaticC0023522
- metachromatic leucodystrophyC0023522
- metachromatic leukodystrophyC0023522
- metachromatic leukoencephalopathyC0023522
- metachromatic leukoencephalyC0023522
- mldC0023522
- sulfatide lipoidosisC0023522
- van Bogaert-Nijssen diseaseC0023522
- Farber's syndromeC2874274
- Other SphingolipidosisC0348489
- Other sphingolipidosisC0348489
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.
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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.