| PDX Collection 6347 (continued) |
| G40309 | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40311 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40319 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G40401 | Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus |
| G40409 | Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40411 | Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40419 | Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G4042 | Cyclin-Dependent Kinase-Like 5 Deficiency Disorder |
| G40501 | Epileptic seizures related to external causes, not intractable, with status epilepticus |
| G40509 | Epileptic seizures related to external causes, not intractable, without status epilepticus |
| G40801 | Other epilepsy, not intractable, with status epilepticus |
| G40802 | Other epilepsy, not intractable, without status epilepticus |
| G40803 | Other epilepsy, intractable, with status epilepticus |
| G40804 | Other epilepsy, intractable, without status epilepticus |
| G40811 | Lennox-Gastaut syndrome, not intractable, with status epilepticus |
| G40812 | Lennox-Gastaut syndrome, not intractable, without status epilepticus |
| G40813 | Lennox-Gastaut syndrome, intractable, with status epilepticus |
| G40814 | Lennox-Gastaut syndrome, intractable, without status epilepticus |
| G40821 | Epileptic spasms, not intractable, with status epilepticus |
| G40822 | Epileptic spasms, not intractable, without status epilepticus |
| G40823 | Epileptic spasms, intractable, with status epilepticus |
| G40824 | Epileptic spasms, intractable, without status epilepticus |
| G40833 | Dravet syndrome, intractable, with status epilepticus |
| G40834 | Dravet syndrome, intractable, without status epilepticus |
| G4089 | Other seizures |
| G40901 | Epilepsy, unspecified, not intractable, with status epilepticus |
| G40909 | Epilepsy, unspecified, not intractable, without status epilepticus |
| G40911 | Epilepsy, unspecified, intractable, with status epilepticus |
| G40919 | Epilepsy, unspecified, intractable, without status epilepticus |
| G40A01 | Absence epileptic syndrome, not intractable, with status epilepticus |
| G40A09 | Absence epileptic syndrome, not intractable, without status epilepticus |
| G40A11 | Absence epileptic syndrome, intractable, with status epilepticus |
| G40A19 | Absence epileptic syndrome, intractable, without status epilepticus |
| G40B01 | Juvenile myoclonic epilepsy, not intractable, with status epilepticus |
| G40B09 | Juvenile myoclonic epilepsy, not intractable, without status epilepticus |
| G40B11 | Juvenile myoclonic epilepsy, intractable, with status epilepticus |
| G40B19 | Juvenile myoclonic epilepsy, intractable, without status epilepticus |
| G40C01 | Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus |
| G40C09 | Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus |
| G40C11 | Lafora progressive myoclonus epilepsy, intractable, with status epilepticus |
| G40C19 | Lafora progressive myoclonus epilepsy, intractable, without status epilepticus |
| G9381 | Temporal sclerosis |
| G9389 | Other specified disorders of brain |
| G939 | Disorder of brain, unspecified |
| G969 | Disorder of central nervous system, unspecified |
| G980 | Neurogenic arthritis, not elsewhere classified |
| G988 | Other disorders of nervous system |
| R561 | Post traumatic seizures |
| |
| PDX Collection 6348 |
| G041 | Tropical spastic paraplegia |
| G10 | Huntington's disease |
| G110 | Congenital nonprogressive ataxia |
| G1110 | Early-onset cerebellar ataxia, unspecified |
| G1111 | Friedreich ataxia |
| G1119 | Other early-onset cerebellar ataxia |
| G112 | Late-onset cerebellar ataxia |
| G113 | Cerebellar ataxia with defective DNA repair |
| G114 | Hereditary spastic paraplegia |
| G115 | Hypomyelination - hypogonadotropic hypogonadism - hypodontia |
| G116 | Leukodystrophy with vanishing white matter disease |
| G118 | Other hereditary ataxias |
| G119 | Hereditary ataxia, unspecified |
| G120 | Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] |
| G121 | Other inherited spinal muscular atrophy |
| G1220 | Motor neuron disease, unspecified |
| G1221 | Amyotrophic lateral sclerosis |
| G1222 | Progressive bulbar palsy |
| G1223 | Primary lateral sclerosis |
| G1224 | Familial motor neuron disease |
| G1225 | Progressive spinal muscle atrophy |
| G1229 | Other motor neuron disease |
| G128 | Other spinal muscular atrophies and related syndromes |
| G129 | Spinal muscular atrophy, unspecified |
| G210 | Malignant neuroleptic syndrome |
| G230 | Hallervorden-Spatz disease |
| G231 | Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] |
| G232 | Striatonigral degeneration |
| G233 | Hypomyelination with atrophy of the basal ganglia and cerebellum |
| G238 | Other specified degenerative diseases of basal ganglia |
| G239 | Degenerative disease of basal ganglia, unspecified |
| G2401 | Drug induced subacute dyskinesia |
| G2402 | Drug induced acute dystonia |
| G2409 | Other drug induced dystonia |
| G241 | Genetic torsion dystonia |
| G242 | Idiopathic nonfamilial dystonia |
| G243 | Spasmodic torticollis |
| G244 | Idiopathic orofacial dystonia |
| G245 | Blepharospasm |
| G248 | Other dystonia |
| G249 | Dystonia, unspecified |
| G250 | Essential tremor |
| G251 | Drug-induced tremor |
| G252 | Other specified forms of tremor |
| G253 | Myoclonus |
| G254 | Drug-induced chorea |
| G255 | Other chorea |
| G2561 | Drug induced tics |
| G2569 | Other tics of organic origin |
| G2570 | Drug induced movement disorder, unspecified |
| G2571 | Drug induced akathisia |
| G2579 | Other drug induced movement disorders |
| G2582 | Stiff-man syndrome |
| G2583 | Benign shuddering attacks |
| G2589 | Other specified extrapyramidal and movement disorders |
| G259 | Extrapyramidal and movement disorder, unspecified |
| G35 | Multiple sclerosis |
| G360 | Neuromyelitis optica [Devic] |
| G361 | Acute and subacute hemorrhagic leukoencephalitis [Hurst] |
| G368 | Other specified acute disseminated demyelination |
| G369 | Acute disseminated demyelination, unspecified |
| G370 | Diffuse sclerosis of central nervous system |
| G371 | Central demyelination of corpus callosum |
| G372 | Central pontine myelinolysis |
| G373 | Acute transverse myelitis in demyelinating disease of central nervous system |
| G375 | Concentric sclerosis [Balo] of central nervous system |
| G3781 | Myelin oligodendrocyte glycoprotein antibody disease |
| G3789 | Other specified demyelinating diseases of central nervous system |
| G379 | Demyelinating disease of central nervous system, unspecified |
| G800 | Spastic quadriplegic cerebral palsy |
| G801 | Spastic diplegic cerebral palsy |
| G802 | Spastic hemiplegic cerebral palsy |
| G803 | Athetoid cerebral palsy |
| G804 | Ataxic cerebral palsy |
| G808 | Other cerebral palsy |
| G809 | Cerebral palsy, unspecified |
| G8100 | Flaccid hemiplegia affecting unspecified side |
| G8101 | Flaccid hemiplegia affecting right dominant side |
| G8102 | Flaccid hemiplegia affecting left dominant side |
| G8103 | Flaccid hemiplegia affecting right nondominant side |
| G8104 | Flaccid hemiplegia affecting left nondominant side |
| G8110 | Spastic hemiplegia affecting unspecified side |
| G8111 | Spastic hemiplegia affecting right dominant side |
| G8112 | Spastic hemiplegia affecting left dominant side |
| G8113 | Spastic hemiplegia affecting right nondominant side |
| G8114 | Spastic hemiplegia affecting left nondominant side |
| G8190 | Hemiplegia, unspecified affecting unspecified side |
| G8191 | Hemiplegia, unspecified affecting right dominant side |
| G8192 | Hemiplegia, unspecified affecting left dominant side |
| G8193 | Hemiplegia, unspecified affecting right nondominant side |
| G8194 | Hemiplegia, unspecified affecting left nondominant side |
| G8220 | Paraplegia, unspecified |
| G8221 | Paraplegia, complete |
| G8222 | Paraplegia, incomplete |
| G8250 | Quadriplegia, unspecified |
| G8251 | Quadriplegia, C1-C4 complete |
| G8252 | Quadriplegia, C1-C4 incomplete |
| G8253 | Quadriplegia, C5-C7 complete |
| G8254 | Quadriplegia, C5-C7 incomplete |
| G830 | Diplegia of upper limbs |
| G8310 | Monoplegia of lower limb affecting unspecified side |
| G8311 | Monoplegia of lower limb affecting right dominant side |
| G8312 | Monoplegia of lower limb affecting left dominant side |
| G8313 | Monoplegia of lower limb affecting right nondominant side |
| G8314 | Monoplegia of lower limb affecting left nondominant side |
| G8320 | Monoplegia of upper limb affecting unspecified side |
| G8321 | Monoplegia of upper limb affecting right dominant side |
| G8322 | Monoplegia of upper limb affecting left dominant side |
| G8323 | Monoplegia of upper limb affecting right nondominant side |
| G8324 | Monoplegia of upper limb affecting left nondominant side |
| G8330 | Monoplegia, unspecified affecting unspecified side |
| G8331 | Monoplegia, unspecified affecting right dominant side |
| G8332 | Monoplegia, unspecified affecting left dominant side |
| G8333 | Monoplegia, unspecified affecting right nondominant side |
| G8334 | Monoplegia, unspecified affecting left nondominant side |
| G834 | Cauda equina syndrome |
| G835 | Locked-in state |
| G8381 | Brown-Sequard syndrome |
| G8382 | Anterior cord syndrome |
| G8383 | Posterior cord syndrome |
| G8384 | Todd's paralysis (postepileptic) |
| G8389 | Other specified paralytic syndromes |
| G839 | Paralytic syndrome, unspecified |
| G9001 | Carotid sinus syncope |
| G9009 | Other idiopathic peripheral autonomic neuropathy |
| G902 | Horner's syndrome |
| G903 | Multi-system degeneration of the autonomic nervous system |
| G904 | Autonomic dysreflexia |
| G9050 | Complex regional pain syndrome I, unspecified |
| G90511 | Complex regional pain syndrome I of right upper limb |
| G90512 | Complex regional pain syndrome I of left upper limb |
| G90513 | Complex regional pain syndrome I of upper limb, bilateral |
| G90519 | Complex regional pain syndrome I of unspecified upper limb |
| G90521 | Complex regional pain syndrome I of right lower limb |
| G90522 | Complex regional pain syndrome I of left lower limb |
| G90523 | Complex regional pain syndrome I of lower limb, bilateral |
| G90529 | Complex regional pain syndrome I of unspecified lower limb |
| G9059 | Complex regional pain syndrome I of other specified site |
| G908 | Other disorders of autonomic nervous system |
| G909 | Disorder of the autonomic nervous system, unspecified |
| G90B | LMNB1-related autosomal dominant leukodystrophy |
| G930 | Cerebral cysts |
| G931 | Anoxic brain damage, not elsewhere classified |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9342 | Megaloencephalic leukoencephalopathy with subcortical cysts |
| G9343 | Leukoencephalopathy with calcifications and cysts |
| G9344 | Adult-onset leukodystrophy with axonal spheroids |
| G9349 | Other encephalopathy |
| G9381 | Temporal sclerosis |
| G9389 | Other specified disorders of brain |
| G939 | Disorder of brain, unspecified |
| G950 | Syringomyelia and syringobulbia |
| G9511 | Acute infarction of spinal cord (embolic) (nonembolic) |
| G9519 | Other vascular myelopathies |
| G9520 | Unspecified cord compression |
| G9529 | Other cord compression |
| G9581 | Conus medullaris syndrome |
| G9589 | Other specified diseases of spinal cord |
| G959 | Disease of spinal cord, unspecified |
| G969 | Disorder of central nervous system, unspecified |
| G980 | Neurogenic arthritis, not elsewhere classified |
| G988 | Other disorders of nervous system |
| I6783 | Posterior reversible encephalopathy syndrome |
| R532 | Functional quadriplegia |
| |
| PDX Collection 6349 |
| E0940 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic neuropathy, unspecified |
| E0941 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic mononeuropathy |
| E0942 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic polyneuropathy |
| E0943 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic autonomic (poly)neuropathy |
| E0944 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic amyotrophy |
| E0949 | Drug or chemical induced diabetes mellitus with neurological complications with other diabetic neurological complication |
| E1040 | Type 1 diabetes mellitus with diabetic neuropathy, unspecified |
| E1041 | Type 1 diabetes mellitus with diabetic mononeuropathy |
| E1042 | Type 1 diabetes mellitus with diabetic polyneuropathy |
| E1043 | Type 1 diabetes mellitus with diabetic autonomic (poly)neuropathy |
| E1044 | Type 1 diabetes mellitus with diabetic amyotrophy |
| E1049 | Type 1 diabetes mellitus with other diabetic neurological complication |
| E1140 | Type 2 diabetes mellitus with diabetic neuropathy, unspecified |
| E1141 | Type 2 diabetes mellitus with diabetic mononeuropathy |
| E1142 | Type 2 diabetes mellitus with diabetic polyneuropathy |
| E1143 | Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy |
| E1144 | Type 2 diabetes mellitus with diabetic amyotrophy |
| E1149 | Type 2 diabetes mellitus with other diabetic neurological complication |
| E1340 | Other specified diabetes mellitus with diabetic neuropathy, unspecified |
| E1341 | Other specified diabetes mellitus with diabetic mononeuropathy |
| E1342 | Other specified diabetes mellitus with diabetic polyneuropathy |
| E1343 | Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy |
| E1344 | Other specified diabetes mellitus with diabetic amyotrophy |
| E1349 | Other specified diabetes mellitus with other diabetic neurological complication |
| G40001 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus |
| G40009 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus |
| G40011 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus |
| G40019 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus |
| G40101 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus |
| G40109 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus |
| G40111 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus |
| G40119 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus |
| G40201 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus |
| G40209 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus |
| G40211 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus |
| G40219 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus |
| G40301 | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus |
| G40309 | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40311 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40319 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G40401 | Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus |
| G40409 | Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40411 | Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40419 | Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G4042 | Cyclin-Dependent Kinase-Like 5 Deficiency Disorder |
| G40501 | Epileptic seizures related to external causes, not intractable, with status epilepticus |
| G40509 | Epileptic seizures related to external causes, not intractable, without status epilepticus |
| G40801 | Other epilepsy, not intractable, with status epilepticus |
| G40802 | Other epilepsy, not intractable, without status epilepticus |
| G40803 | Other epilepsy, intractable, with status epilepticus |
| G40804 | Other epilepsy, intractable, without status epilepticus |
| G40811 | Lennox-Gastaut syndrome, not intractable, with status epilepticus |
| G40812 | Lennox-Gastaut syndrome, not intractable, without status epilepticus |
| G40813 | Lennox-Gastaut syndrome, intractable, with status epilepticus |
| G40814 | Lennox-Gastaut syndrome, intractable, without status epilepticus |
| G40821 | Epileptic spasms, not intractable, with status epilepticus |
| G40822 | Epileptic spasms, not intractable, without status epilepticus |
| G40823 | Epileptic spasms, intractable, with status epilepticus |
| G40824 | Epileptic spasms, intractable, without status epilepticus |
| G40833 | Dravet syndrome, intractable, with status epilepticus |
| G40834 | Dravet syndrome, intractable, without status epilepticus |
| G4089 | Other seizures |
| G40901 | Epilepsy, unspecified, not intractable, with status epilepticus |
| G40909 | Epilepsy, unspecified, not intractable, without status epilepticus |
| G40911 | Epilepsy, unspecified, intractable, with status epilepticus |
| G40919 | Epilepsy, unspecified, intractable, without status epilepticus |
| G40A01 | Absence epileptic syndrome, not intractable, with status epilepticus |
| G40A09 | Absence epileptic syndrome, not intractable, without status epilepticus |
| G40A11 | Absence epileptic syndrome, intractable, with status epilepticus |
| G40A19 | Absence epileptic syndrome, intractable, without status epilepticus |
| G40B01 | Juvenile myoclonic epilepsy, not intractable, with status epilepticus |
| G40B09 | Juvenile myoclonic epilepsy, not intractable, without status epilepticus |
| G40B11 | Juvenile myoclonic epilepsy, intractable, with status epilepticus |
| G40B19 | Juvenile myoclonic epilepsy, intractable, without status epilepticus |
| G40C01 | Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus |
| G40C09 | Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus |
| G40C11 | Lafora progressive myoclonus epilepsy, intractable, with status epilepticus |
| G40C19 | Lafora progressive myoclonus epilepsy, intractable, without status epilepticus |
| G9381 | Temporal sclerosis |
| G9389 | Other specified disorders of brain |
| G939 | Disorder of brain, unspecified |
| G969 | Disorder of central nervous system, unspecified |
| G980 | Neurogenic arthritis, not elsewhere classified |
| G988 | Other disorders of nervous system |
| R561 | Post traumatic seizures |
| |
| PDX Collection 6350 |
| C880 | Waldenstrom macroglobulinemia |
| D472 | Monoclonal gammopathy |
| D890 | Polyclonal hypergammaglobulinemia |
| D891 | Cryoglobulinemia |
| E700 | Classical phenylketonuria |
| E701 | Other hyperphenylalaninemias |
| E7020 | Disorder of tyrosine metabolism, unspecified |
| E7021 | Tyrosinemia |
| E7029 | Other disorders of tyrosine metabolism |
| E7030 | Albinism, unspecified |
| E70310 | X-linked ocular albinism |
| E70311 | Autosomal recessive ocular albinism |
| E70318 | Other ocular albinism |
| E70319 | Ocular albinism, unspecified |
| E70320 | Tyrosinase negative oculocutaneous albinism |
| E70321 | Tyrosinase positive oculocutaneous albinism |
| E70328 | Other oculocutaneous albinism |
| E70329 | Oculocutaneous albinism, unspecified |
| E70330 | Chediak-Higashi syndrome |
| E70331 | Hermansky-Pudlak syndrome |
| E70338 | Other albinism with hematologic abnormality |
| E70339 | Albinism with hematologic abnormality, unspecified |
| E7039 | Other specified albinism |
| E7040 | Disorders of histidine metabolism, unspecified |
| E7041 | Histidinemia |
| E7049 | Other disorders of histidine metabolism |
| E705 | Disorders of tryptophan metabolism |
| E7081 | Aromatic L-amino acid decarboxylase deficiency |
| E7089 | Other disorders of aromatic amino-acid metabolism |
| E709 | Disorder of aromatic amino-acid metabolism, unspecified |
| E710 | Maple-syrup-urine disease |
| E71110 | Isovaleric acidemia |
| E71111 | 3-methylglutaconic aciduria |
| E71118 | Other branched-chain organic acidurias |
| E71120 | Methylmalonic acidemia |
| E71121 | Propionic acidemia |
| E71128 | Other disorders of propionate metabolism |
| E7119 | Other disorders of branched-chain amino-acid metabolism |
| E712 | Disorder of branched-chain amino-acid metabolism, unspecified |
| E7130 | Disorder of fatty-acid metabolism, unspecified |
| E7200 | Disorders of amino-acid transport, unspecified |
| E7201 | Cystinuria |
| E7202 | Hartnup's disease |
| E7204 | Cystinosis |
| E7209 | Other disorders of amino-acid transport |
| E7210 | Disorders of sulfur-bearing amino-acid metabolism, unspecified |
| E7211 | Homocystinuria |
| E7212 | Methylenetetrahydrofolate reductase deficiency |
| E7219 | Other disorders of sulfur-bearing amino-acid metabolism |
| E7220 | Disorder of urea cycle metabolism, unspecified |
| E7221 | Argininemia |
| E7222 | Arginosuccinic aciduria |
| E7223 | Citrullinemia |
| E7229 | Other disorders of urea cycle metabolism |
| E723 | Disorders of lysine and hydroxylysine metabolism |
| E724 | Disorders of ornithine metabolism |
| E7250 | Disorder of glycine metabolism, unspecified |
| E7251 | Non-ketotic hyperglycinemia |
| E7252 | Trimethylaminuria |
| E7253 | Primary hyperoxaluria |
| E7259 | Other disorders of glycine metabolism |
| E7281 | Disorders of gamma aminobutyric acid metabolism |
| E7289 | Other specified disorders of amino-acid metabolism |
| E729 | Disorder of amino-acid metabolism, unspecified |
| E730 | Congenital lactase deficiency |
| E731 | Secondary lactase deficiency |
| E738 | Other lactose intolerance |
| E739 | Lactose intolerance, unspecified |
| E7400 | Glycogen storage disease, unspecified |
| E7401 | von Gierke disease |
| E7402 | Pompe disease |
| E7403 | Cori disease |
| E7404 | McArdle disease |
| E7405 | Lysosome-associated membrane protein 2 [LAMP2] deficiency |
| E7409 | Other glycogen storage disease |
| E7410 | Disorder of fructose metabolism, unspecified |
| E7411 | Essential fructosuria |
| E7412 | Hereditary fructose intolerance |
| E7419 | Other disorders of fructose metabolism |
| E7420 | Disorders of galactose metabolism, unspecified |
| E7421 | Galactosemia |
| E7429 | Other disorders of galactose metabolism |
| E7431 | Sucrase-isomaltase deficiency |
| E7439 | Other disorders of intestinal carbohydrate absorption |
| E744 | Disorders of pyruvate metabolism and gluconeogenesis |
| E74810 | Glucose transporter protein type 1 deficiency |
| E74818 | Other disorders of glucose transport |
| E74819 | Disorders of glucose transport, unspecified |
| E7489 | Other specified disorders of carbohydrate metabolism |
| E749 | Disorder of carbohydrate metabolism, unspecified |
| E7521 | Fabry (-Anderson) disease |
| E7522 | Gaucher disease |
| E75240 | Niemann-Pick disease type A |
| E75241 | Niemann-Pick disease type B |
| E75242 | Niemann-Pick disease type C |
| E75243 | Niemann-Pick disease type D |
| E75248 | Other Niemann-Pick disease |
| E75249 | Niemann-Pick disease, unspecified |
| E753 | Sphingolipidosis, unspecified |
| E755 | Other lipid storage disorders |
| E756 | Lipid storage disorder, unspecified |
| E770 | Defects in post-translational modification of lysosomal enzymes |
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