E75.4
BillableNeuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Batten disease
- Bielschowsky-Jansky disease
- Kufs disease
- Spielmeyer-Vogt disease
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)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Cerebral degeneration in childhood2584003
- Amaurotic idiocy early juvenile type14637005
- Amaurotic idiocy late infantile type14637005
- Amaurotic idiocy, early juvenile type14637005
- Amaurotic idiocy, late infantile type14637005
- Bielschowsky-Jansky disease14637005
- Bielschowsky-Jansky type neuronal ceroid lipofuscinosis14637005
- Dollinger-Bielschowsky syndrome14637005
- Dollinger-Bielschowsky type neuronal ceroid lipofuscinosis14637005
- Late infantile neuronal ceroid lipofuscinosis14637005
- Late-infantile neuronal ceroid lipofuscinosis14637005
- Cerebral lipidosis16517004
- Cerebromacular degeneration42012007
- Cerebromacular dystrophy42012007
- Neuronal ceroid lipofuscinosis42012007
- Pigmentary retinal lipoid neuronal heredodegeneration42012007
- Hagberg-Santavouri type neuronal ceroid lipofuscinosis58258004
- Hagberg-Santavuori disease58258004
- Haltia-Santavouri type neuronal ceroid lipofuscinosis58258004
- Infantile neuronal ceroid lipofuscinosis58258004
- Neuronal ceroid lipofuscinosis infantile Finnish type58258004
- Neuronal ceroid lipofuscinosis, infantile Finnish type58258004
- Polyunsaturated acid lipidosis58258004
- Polyunsaturated fatty acid lipidosis58258004
- Santavuori disease58258004
- Amaurotic idiocy juvenile type61663001
- Amaurotic idiocy, juvenile type61663001
- Batten-Mayou disease61663001
- Batten-Mayou syndrome61663001
- Batten-Spielmeyer-Vogt disease61663001
- Cerebral lipidosis myoclonic variant61663001
- Cerebral lipidosis, myoclonic variant61663001
- Juvenile neuronal ceroid lipofuscinosis61663001
- Spielmeyer-Vogt disease61663001
- Spielmeyer-Vogt type neuronal ceroid lipofuscinosis61663001
- Adult neuronal ceroid lipofuscinosis62009002
- Adult-type amaurotic idiocy62009002
- Amaurotic idiocy adult type62009002
- Amaurotic idiocy late familial62009002
- Kufs type neuronal ceroid lipofuscinosis62009002
- Kufs' disease62009002
- Late familial amaurotic idiocy62009002
- Dementia associated with cerebral lipidosis698624003
- Neuronal ceroid lipofuscinosis 8703526007
- Northern epilepsy703526007
- Progressive epilepsy with mental retardation703526007
- Progressive epilepsy-intellectual disability syndrome Finnish type703526007
- Cathepsin D deficient neuronal ceroid lipofuscinosis720830009
- Congenital neuronal ceroid lipofuscinosis720830009
- Neuronal ceroid lipofuscinosis 10720830009
- Neuronal ceroid lipofuscinosis due to cathepsin D deficiency720830009
- Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D720830009
- Acquired ataxia722968003
- ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis789657008
- CLN12 disease789657008
- Juvenile parkinsonism, neuronal ceroid lipofuscinosis789657008
- Myoclonic disorder due to neuronal ceroid lipofuscinosis1263506002
- CLN6 transmembrane ER protein-related neuronal ceroid lipofuscinosis type 6A1296784002
- CLN6-related neuronal ceroid lipofuscinosis type 6A1296784002
- Neuronal ceroid lipofuscinosis type 6A1296784002
- vLINCL - variant late infantile neuronal ceroid lipofuscinosis1296784002
UMLS
- Adult Neuronal Ceroid LipofuscinosisC0022797
- Adult neuronal ceroid lipofuscinosisC0022797
- Adult neuronal ceroid lipofuscinosis (disorder)C0022797
- Adult-type amaurotic idiocyC0022797
- Amaurotic Idiocy, Adult TypeC0022797
- Amaurotic idiocy adult typeC0022797
- Amaurotic idiocy late familialC0022797
- Ceroid Lipofuscinosis, Neuronal 4C0022797
- Disease, Kuf'sC0022797
- KUFS DISC0022797
- Kuf DiseaseC0022797
- Kuf's DiseaseC0022797
- Kufs DiseaseC0022797
- Kufs Type Neuronal Ceroid LipofuscinosisC0022797
- Kufs diseaseC0022797
- Kufs type neuronal ceroid lipofuscinosisC0022797
- Kufs' diseaseC0022797
- Late familial amaurotic idiocyC0022797
- Neuronal Ceroid Lipofuscinosis, AdultC0022797
- Neuronal Ceroid Lipofuscinosis, Adult TypeC0022797
- kuf diseaseC0022797
- kuf's diseaseC0022797
- kufs diseaseC0022797
- kufs' diseaseC0022797
- Amaurotic idiocy early juvenile typeC0022340
- Amaurotic idiocy late infantile typeC0022340
- Amaurotic idiocy, early juvenile typeC0022340
- Amaurotic idiocy, late infantile typeC0022340
- Bielschowsky-Jansky diseaseC0022340
- Bielschowsky-Jansky type neuronal ceroid lipofuscinosisC0022340
- Dollinger-Bielschowsky syndromeC0022340
- Dollinger-Bielschowsky type neuronal ceroid lipofuscinosisC0022340
- JANSKY BIELSCHOWSKY DISC0022340
- Jansky Bielschowsky DiseaseC0022340
- Jansky-Bielschowsky DiseaseC0022340
- Jansky-Bielschowsky diseaseC0022340
- LINCLC0022340
- Late infantile neuronal ceroid lipofuscinosisC0022340
- Late-Infantile Neuronal Ceroid LipofuscinosisC0022340
- Late-infantile Batten diseaseC0022340
- Late-infantile neuronal ceroid lipofuscinosisC0022340
- Late-infantile neuronal ceroid lipofuscinosis (disorder)C0022340
- Neuronal Ceroid Lipofuscinosis, Late InfantileC0022340
- Neuronal Ceroid Lipofuscinosis, Late-InfantileC0022340
- Neuronal ceroid lipofuscinosis, late-infantileC0022340
- bielschowsky disease janskyC0022340
- jansky-bielschowsky diseaseC0022340
- Amaurotic idiocy juvenile typeC0751383
- Amaurotic idiocy, juvenile typeC0751383
- BATTEN DISC0751383
- BATTEN DISEASEC0751383
- BATTEN MAYOU DISC0751383
- BATTEN SPIELMEYER VOGT DISC0751383
- Batten DiseaseC0751383
- Batten Disease, JuvenileC0751383
- Batten Diseases, JuvenileC0751383
- Batten Mayou DiseaseC0751383
- Batten Spielmeyer Vogt DiseaseC0751383
- Batten diseaseC0751383
- Batten's diseaseC0751383
- Batten's syndromeC0751383
- Batten-Mayou DiseaseC0751383
- Batten-Mayou diseaseC0751383
- Batten-Mayou syndromeC0751383
- Batten-Spielmeyer-Vogt DiseaseC0751383
- Batten-Spielmeyer-Vogt diseaseC0751383
- CEROID LIPOFUSCINOSIS, NEURONAL, 3C0751383
- CLN3C0751383
- CLN3 Related Neuronal Ceroid LipofuscinosisC0751383
- CLN3 diseaseC0751383
- CLN3-Related Neuronal Ceroid-LipofuscinosesC0751383
- CLN3-Related Neuronal Ceroid-LipofuscinosisC0751383
- CLN3-related neuronal ceroid-lipofuscinosisC0751383
- Cerebral lipidosis myoclonic variantC0751383
- Cerebral lipidosis, myoclonic variantC0751383
- Cerebroretinal Degeneration, JuvenileC0751383
- Cerebroretinal Degenerations, JuvenileC0751383
- Ceroid Lipofuscinosis, Neuronal 3, JuvenileC0751383
- Ceroid Lipofuscinosis, Neuronal, 3C0751383
- Ceroid-Lipofuscinosis, CLN3-Related NeuronalC0751383
- Disease, Juvenile BattenC0751383
- Disease, Spielmeyer-SjogrenC0751383
- Disease, Vogt SpielmeyerC0751383
- Disease, Vogt-SpielmeyerC0751383
- JNCLC0751383
- Juvenile Batten DiseaseC0751383
- Juvenile Batten DiseasesC0751383
- Juvenile Batten diseaseC0751383
- Juvenile Cerebroretinal DegenerationC0751383
- Juvenile Cerebroretinal DegenerationsC0751383
- Juvenile Neuronal Ceroid LipofuscinosisC0751383
- Juvenile cerebroretinal degenerationC0751383
- Juvenile neuronal ceroid lipofuscinosisC0751383
- Juvenile neuronal ceroid lipofuscinosis (disorder)C0751383
- NEURONAL CEROID LIPOFUSCINOSIS, JUVENILEC0751383
- Neuronal Ceroid Lipofuscinosis Juvenile TypeC0751383
- Neuronal Ceroid Lipofuscinosis Type 3C0751383
- Neuronal Ceroid Lipofuscinosis, JuvenileC0751383
- Neuronal Ceroid-Lipofuscinoses, CLN3-RelatedC0751383
- Neuronal Ceroid-Lipofuscinosis, CLN3-RelatedC0751383
- SPIELMEYER VOGT DISC0751383
- SPIELMEYER-SJOGREN DISEASEC0751383
- Spielmeyer Disease, VogtC0751383
- Spielmeyer Sjogren DiseaseC0751383
- Spielmeyer Vogt DiseaseC0751383
- Spielmeyer-Sjogren DiseaseC0751383
- Spielmeyer-Vogt DiseaseC0751383
- Spielmeyer-Vogt diseaseC0751383
- Spielmeyer-Vogt type neuronal ceroid lipofuscinosisC0751383
- VOGT-SPIELMEYER DISEASEC0751383
- Vogt Spielmeyer DiseaseC0751383
- Vogt Spielmeyer diseaseC0751383
- Vogt-Spielmeyer DiseaseC0751383
- Vogt-Spielmeyer diseaseC0751383
- batten diseaseC0751383
- batten's diseaseC0751383
- batten's syndromeC0751383
- battens diseaseC0751383
- spielmeyer-vogt diseaseC0751383
- Cerebromacular degenerationC0027877
- Cerebromacular dystrophyC0027877
- Ceroid Lipofuscinosis, NeuronalC0027877
- Ceroid Storage DiseaseC0027877
- Ceroid Storage DiseasesC0027877
- Ceroid-Lipofuscinosis, NeuronalC0027877
- Disease, Ceroid StorageC0027877
- Disease, Lipofuscin StorageC0027877
- Lipofuscin Storage DiseaseC0027877
- Lipofuscin Storage DiseasesC0027877
- Lipofuscinosis, Neuronal CeroidC0027877
- Neuronal Ceroid LipofuscinosesC0027877
- Neuronal Ceroid LipofuscinosisC0027877
- Neuronal Ceroid-LipofuscinosesC0027877
- Neuronal Ceroid-LipofuscinosisC0027877
- Neuronal ceroid lipofuscinosisC0027877
- Neuronal ceroid lipofuscinosis (disorder)C0027877
- Neuronal ceroid lipofuscinosis NOSC0027877
- Pigmentary retinal lipoid neuronal heredodegenerationC0027877
- Storage Disease, CeroidC0027877
- Storage Disease, LipofuscinC0027877
- ceroid lipofuscinoses neuronalC0027877
- ceroid lipofuscinosisC0027877
- hereditary ceroid lipofuscinosisC0027877
- neuronal ceroid lipofuscinosesC0027877
- neuronal ceroid lipofuscinosisC0027877
- neuronal ceroid-lipofuscinosisC0027877
Frequently Asked Questions
What is ICD-10 code E75.4?
ICD-10-CM code E75.4 represents "Neuronal ceroid lipofuscinosis". It is a billable/specific code that can be used on a claim.
Is E75.4 a billable code?
Yes, E75.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.4 in?
E75.4 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.4?
E75.4 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 5 more.
What SNOMED CT codes does E75.4 map to?
E75.4 maps to 14 SNOMED CT concepts: 789657008, 722968003, 62009002, 14637005, 61663001, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.4?
E75.4 is linked to 4 UMLS Concept Unique Identifiers: C0022797, C0022340, C0751383, C0027877. 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.