| PDX Collection 6120 (continued) |
| G804 | Ataxic cerebral palsy |
| G808 | Other cerebral palsy |
| G809 | Cerebral palsy, unspecified |
| 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 |
| 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 |
| G935 | Compression of brain |
| G936 | Cerebral edema |
| 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 |
| I6783 | Posterior reversible encephalopathy syndrome |
| R532 | Functional quadriplegia |
| |
| PDX Collection 6121 |
| 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 |
| 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 |
| G939 | Disorder of brain, 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 |
| R561 | Post traumatic seizures |
| |
| PDX Collection 6122 |
| E7500 | GM2 gangliosidosis, unspecified |
| E7501 | Sandhoff disease |
| E7502 | Tay-Sachs disease |
| E7509 | Other GM2 gangliosidosis |
| E7510 | Unspecified gangliosidosis |
| E7511 | Mucolipidosis IV |
| E7519 | Other gangliosidosis |
| E7523 | Krabbe disease |
| E7525 | Metachromatic leukodystrophy |
| E7526 | Sulfatase deficiency |
| E7527 | Pelizaeus-Merzbacher disease |
| E7528 | Canavan disease |
| E7529 | Other sphingolipidosis |
| E754 | Neuronal ceroid lipofuscinosis |
| F842 | Rett's syndrome |
| G312 | Degeneration of nervous system due to alcohol |
| G3181 | Alpers disease |
| G3182 | Leigh's disease |
| 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 |
| |
| PDX Collection 6123 |
| 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 |
| 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 |
| G939 | Disorder of brain, 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 |
| R561 | Post traumatic seizures |
| |
| PDX Collection 6124 |
| I2101 | ST elevation (STEMI) myocardial infarction involving left main coronary artery |
| I2102 | ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery |
| I2109 | ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall |
| I2111 | ST elevation (STEMI) myocardial infarction involving right coronary artery |
| I2119 | ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall |
| I2121 | ST elevation (STEMI) myocardial infarction involving left circumflex coronary artery |
| I2129 | ST elevation (STEMI) myocardial infarction involving other sites |
| I213 | ST elevation (STEMI) myocardial infarction of unspecified site |
| I214 | Non-ST elevation (NSTEMI) myocardial infarction |
| I219 | Acute myocardial infarction, unspecified |
| I21A1 | Myocardial infarction type 2 |
| I21A9 | Other myocardial infarction type |
| I21B | Myocardial infarction with coronary microvascular dysfunction |
| I220 | Subsequent ST elevation (STEMI) myocardial infarction of anterior wall |
| I221 | Subsequent ST elevation (STEMI) myocardial infarction of inferior wall |
| I222 | Subsequent non-ST elevation (NSTEMI) myocardial infarction |
| I228 | Subsequent ST elevation (STEMI) myocardial infarction of other sites |
| I229 | Subsequent ST elevation (STEMI) myocardial infarction of unspecified site |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| |
| PDX Collection 6125 |
| I2101 | ST elevation (STEMI) myocardial infarction involving left main coronary artery |
| I2102 | ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery |
| I2109 | ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall |
| I2111 | ST elevation (STEMI) myocardial infarction involving right coronary artery |
| I2119 | ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall |
| I2121 | ST elevation (STEMI) myocardial infarction involving left circumflex coronary artery |
| I2129 | ST elevation (STEMI) myocardial infarction involving other sites |
| I213 | ST elevation (STEMI) myocardial infarction of unspecified site |
| I214 | Non-ST elevation (NSTEMI) myocardial infarction |
| I219 | Acute myocardial infarction, unspecified |
| I21A1 | Myocardial infarction type 2 |
| I21A9 | Other myocardial infarction type |
| I21B | Myocardial infarction with coronary microvascular dysfunction |
| I220 | Subsequent ST elevation (STEMI) myocardial infarction of anterior wall |
| I221 | Subsequent ST elevation (STEMI) myocardial infarction of inferior wall |
| I222 | Subsequent non-ST elevation (NSTEMI) myocardial infarction |
| I228 | Subsequent ST elevation (STEMI) myocardial infarction of other sites |
| I229 | Subsequent ST elevation (STEMI) myocardial infarction of unspecified site |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| |
| PDX Collection 6126 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8843 | Disorders of mitochondrial tRNA synthetases |
| E8849 | Other mitochondrial metabolism disorders |
| E8889 | Other specified metabolic disorders |
| |
| PDX Collection 6127 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8841 | MELAS syndrome |
| E88811 | Insulin resistance syndrome, Type A |
| E88818 | Other insulin resistance |
| E88819 | Insulin resistance, unspecified |
| E8889 | Other specified metabolic disorders |
| |
| PDX Collection 6128 |
| E7500 | GM2 gangliosidosis, unspecified |
| E7501 | Sandhoff disease |
| E7502 | Tay-Sachs disease |
| E7509 | Other GM2 gangliosidosis |
| E7510 | Unspecified gangliosidosis |
| E7511 | Mucolipidosis IV |
| E7519 | Other gangliosidosis |
| E754 | Neuronal ceroid lipofuscinosis |
| F842 | Rett's syndrome |
| G300 | Alzheimer's disease with early onset |
| G301 | Alzheimer's disease with late onset |
| G308 | Other Alzheimer's disease |
| G309 | Alzheimer's disease, unspecified |
| G3101 | Pick's disease |
| G3109 | Other frontotemporal neurocognitive disorder |
| G311 | Senile degeneration of brain, not elsewhere classified |
| G312 | Degeneration of nervous system due to alcohol |
| G3180 | Leukodystrophy, unspecified |
| G3181 | Alpers disease |
| G3182 | Leigh's disease |
| G3184 | Mild cognitive impairment of uncertain or unknown etiology |
| G3185 | Corticobasal degeneration |
| G3186 | Alexander disease |
| G3189 | Other specified degenerative diseases of nervous system |
| G319 | Degenerative disease of nervous system, unspecified |
| |
| PDX Collection 6129 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8842 | MERRF syndrome |
| E88811 | Insulin resistance syndrome, Type A |
| E88818 | Other insulin resistance |
| E88819 | Insulin resistance, unspecified |
| E8889 | Other specified metabolic disorders |
| |
| PDX Collection 6130 |
| E7500 | GM2 gangliosidosis, unspecified |
| E7501 | Sandhoff disease |
| E7502 | Tay-Sachs disease |
| E7509 | Other GM2 gangliosidosis |
| E7510 | Unspecified gangliosidosis |
| E7511 | Mucolipidosis IV |
| E7519 | Other gangliosidosis |
| E754 | Neuronal ceroid lipofuscinosis |
| F842 | Rett's syndrome |
| G300 | Alzheimer's disease with early onset |
| G301 | Alzheimer's disease with late onset |
| G308 | Other Alzheimer's disease |
| G309 | Alzheimer's disease, unspecified |
| G3101 | Pick's disease |
| G3109 | Other frontotemporal neurocognitive disorder |
| G311 | Senile degeneration of brain, not elsewhere classified |
| G312 | Degeneration of nervous system due to alcohol |
| G3180 | Leukodystrophy, unspecified |
| G3181 | Alpers disease |
| G3182 | Leigh's disease |
| G3184 | Mild cognitive impairment of uncertain or unknown etiology |
| G3185 | Corticobasal degeneration |
| G3186 | Alexander disease |
| G3189 | Other specified degenerative diseases of nervous system |
| G319 | Degenerative disease of nervous system, unspecified |
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