Specific code 2014 ICD-9-CM Diagnosis Code 330.1
Cerebral lipidoses
  • Billable Code
  • ICD-9-CM 330.1 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM 330.1 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
Disease Synonyms
  • Adult neuronal ceroid lipofuscinosis (disorder)
  • Cerebral lipidosis
  • Gangliosidosis
  • GM>2< gangliosidosis
  • GM2 gangliosidosis
  • Juvenile neuronal ceroid lipofuscinosis (disorder)
  • Lipofuscinosis, neuronal ceroid, adult
  • Lipofuscinosis, neuronal ceroid, juvenile
  • Neuronal ceroid lipofuscinosis
  • Neuronal ceroid lipofuscinosis, adult
  • Neuronal ceroid lipofuscinosis, juvenile
  • Sandhoff disease
  • Tay Sachs disease
  • Tay-Sachs disease (disorder)
Clinical Information
  • Autosomal recessive inherited gangliosidosis characterized by the onset in the first 6 months of life of an exaggerated startle response, delay in psychomotor development, hypotonia (followed by spasticity), visual loss, and a macular cherry red spot; hexosaminidase a is deficient, leading to the accumulation of gm2 ganglioside in neurons of the central nervous system and retina; this condition is strongly associated with ashkenazic jewish ancestry.
  • Group of often fatal inherited diseases marked by the accumulation of gangliosides in lysosomes secondary to enzymatic deficiency states; gangliosidoses include tay-sachs disease, gangliosidosis gm1, gangliosidoses gm2, and sandhoff disease; which share the infantile or childhood onset of central nervous system deterioration.
Applies To
  • Amaurotic (familial) idiocy
  • Disease:
    • Batten
    • Jansky-Bielschowsky
    • Kufs'
    • Spielmeyer-Vogt
    • Tay-Sachs
    • Gangliosidosis
Convert to ICD-10-CM: 330.1 converts approximately to:
  • 2014 ICD-10-CM E75.02 Tay-Sachs disease
    Or:
  • 2014 ICD-10-CM E75.19 Other gangliosidosis
    Or:
  • 2014 ICD-10-CM E75.4 Neuronal ceroid lipofuscinosis
ICD-9-CM Volume 2 Index entries containing back-references to 330.1:
  • Amaurotic familial idiocy (infantile) (juvenile) (late) 330.1
  • Bielschowsky's disease 330.1
  • Bielschowsky-Jansky
    • amaurotic familial idiocy 330.1
    • disease 330.1
  • Cerebromacular degeneration 330.1
  • Degeneration, degenerative
    • cerebromacular 330.1
  • Disease, diseased - see also Syndrome
    • Bielschowsky (-Jansky) 330.1
    • Jansky-Bielschowsky 330.1
    • Kufs' 330.1
    • Sachs (-Tay) 330.1
    • Sandhoff's 330.1
    • Spielmeyer-Stock 330.1
    • Spielmeyer-Vogt 330.1
    • Tay-Sachs 330.1
    • Vogt-Spielmeyer 330.1
  • Gangliosidosis 330.1
  • Idiot, idiocy (congenital) 318.2
    • amaurotic (Bielschowsky) (-Jansky) (family) (infantile (late)) (juvenile (late)) (Vogt-Spielmeyer) 330.1
  • Jansky-Bielschowsky amaurotic familial idiocy 330.1
  • Kufs' disease 330.1
  • Lipidosis 272.7
    • cerebral (infantile) (juvenile) (late) 330.1
  • Sachs (-Tay) disease (amaurotic familial idiocy) 330.1
  • Sandhoff's disease 330.1
  • Spielmeyer-Stock disease 330.1
  • Spielmeyer-Vogt disease 330.1
  • Tay-Sachs
    • amaurotic familial idiocy 330.1
    • disease 330.1
  • Vogt-Spielmeyer disease (amaurotic familial idiocy) 330.1
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 330.1 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2014 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.