HEREDITARY AND DEGENERATIVE DISEASES OF THE CENTRAL NERVOUS SYSTEM (330-337)
Excludes:
hepatolenticular degeneration (275.1)
multiple sclerosis (340)
other demyelinating diseases of central nervous system (341.0-341.9)
330 Cerebral degenerations usually manifest in childhood
Use additional code to identify associated intellectual disabilities
Krabbe's disease
Leukodystrophy:
NOS
globoid cell
metachromatic
sudanophilic
Pelizaeus-Merzbacher disease
Sulfatide lipidosis
Amaurotic (familial) idiocy
Disease:
Batten
Jansky-Bielschowsky
Kufs'
Spielmeyer-Vogt
Tay-Sachs
Gangliosidosis
Code first underlying disease, as:
Fabry's disease (272.7)
Gaucher's disease (272.7)
Niemann-Pick disease (272.7)
sphingolipidosis (272.7)
Code first underlying disease, as:
Hunter's disease (277.5)
mucopolysaccharidosis (277.5)
Alpers' disease or gray-matter degeneration
Infantile necrotizing encephalomyelopathy
Leigh's disease
Subacute necrotizing encephalopathy or encephalomyelopathy

Home