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ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual |
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Appendix C: Principal diagnoses which convert CC/MCC to non-CC |
Page 1144 of 1375 |
PDX Collection 6119 | |
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 6120 | |
G041 | Tropical spastic paraplegia |
G10 | Huntington's disease |
G1222 | Progressive bulbar palsy |
G20A1 | Parkinson's disease without dyskinesia, without mention of fluctuations |
G20A2 | Parkinson's disease without dyskinesia, with fluctuations |
G20B1 | Parkinson's disease with dyskinesia, without mention of fluctuations |
G20B2 | Parkinson's disease with dyskinesia, with fluctuations |
G20C | Parkinsonism, unspecified |
G210 | Malignant neuroleptic syndrome |
G2111 | Neuroleptic induced parkinsonism |
G2119 | Other drug induced secondary parkinsonism |
G212 | Secondary parkinsonism due to other external agents |
G213 | Postencephalitic parkinsonism |
G214 | Vascular parkinsonism |
G218 | Other secondary parkinsonism |
G219 | Secondary parkinsonism, 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 |
G26 | Extrapyramidal and movement disorders in diseases classified elsewhere |
G3289 | Other specified degenerative disorders of nervous system in diseases classified elsewhere |
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 |
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 |
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 |
G998 | Other specified disorders of nervous system in diseases classified elsewhere |
I6783 | Posterior reversible encephalopathy syndrome |
R532 | Functional quadriplegia |
PDX Collection 6121 | |
G3289 | Other specified degenerative disorders of nervous system in diseases classified elsewhere |
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 |
G998 | Other specified disorders of nervous system in diseases classified elsewhere |
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 | |
G3289 | Other specified degenerative disorders of nervous system in diseases classified elsewhere |
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 |
G998 | Other specified disorders of nervous system in diseases classified elsewhere |
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 |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |