POMS Reference
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POMS changes on March 29, 2018
DI 23022.095: Alexander Disease
DI 23022.130: Canavan Disease
DI 23022.141: Coffin-Lowry Syndrome
DI 23022.145: Creutzfeldt-Jakob Disease (CJD)
DI 23022.160: Farber's Disease
DI 23022.165: Friedreich's Ataxia (FRDA)
DI 23022.170: Frontotemporal Dementia (FTD), Pick's Disease -Type A
DI 23022.181: Giant Axonal Neuropathy
DI 23022.190: Head and Neck Cancers
DI 23022.191: Hoyeraal-Hreidarsson Syndrome
DI 23022.195: Infantile Neuroaxonal Dystrophy (INAD)
DI 23022.202: Joubert Syndrome
DI 23022.210: Krabbe Disease (KD) - Infantile
DI 23022.220: Lesch-Nyhan Syndrome (LNS)
DI 23022.235: Metachromatic Leukodystrophy (MLD)
DI 23022.250: Ornithine Transcarbamylase (OTC) Deficiency
DI 23022.261: Pallister-Killian Syndrome
DI 23022.280: Pompe Disease - Infantile
DI 23022.281: Progressive Bulbar Palsy
DI 23022.285: Rett (RTT) Syndrome
DI 23022.296: Seckel Syndrome
DI 23022.297: Sjogren-Larsson Syndrome
DI 23022.300: Small Cell Cancer of the Large Intestine
DI 23022.330: Spinal Muscular Atrophy (SMA) - Types 0 and 1
DI 23022.347: X-Linked Myotubular Myopathy
DI 23022.360: Ataxia Telangiectasia
DI 23022.365: Batten Disease
DI 23022.385: Early-Onset Alzheimer's Disease
DI 23022.400: Fukuyama Congenital Muscular Dystrophy
DI 23022.425: Infantile Neuronal Ceroid-Lipofuscinoses
DI 23022.435: Late Infantile Neuronal Ceroid-Lipofuscinoses
DI 23022.445: Maple Syrup Urine Disease
DI 23022.450: Merosin Deficient Congenital Muscular Dystrophy
DI 23022.455: Mixed Dementia
DI 23022.490: Progressive Multifocal Leukoencephalopathy
DI 23022.505: Subacute Sclerosing Panencephalitis
DI 23022.520: Ullrich Congenital Muscular Dystrophy
DI 23022.525: Walker Warburg Syndrome
DI 23022.600: Angelman Syndrome
DI 23022.605: Corticobasal Degeneration
DI 23022.610: Lewy Body Dementia
DI 23022.620: Malignant Multiple Sclerosis
DI 23022.625: Multicentric Castleman Disease
DI 23022.630: Multiple System Atrophy
DI 23022.640: Primary Central Nervous System Lymphoma
DI 23022.645: Primary Effusion Lymphoma
DI 23022.650: Progressive Supranuclear Palsy
DI 23022.655: Pulmonary Kaposi Sarcoma
DI 23022.660: The ALS Parkinsonism Dementia Complex
DI 23022.665: Aicardi--Goutieres Syndrome
DI 23022.675: Alpers Disease
DI 23022.680: Alpha Mannosidosis--Type II and III
DI 23022.690: Cerebrotendinous Xanthomatosis
DI 23022.785: Juvenile Onset Huntington Disease
DI 23022.790: Kufs Disease--Type A and B
DI 23022.795: Lissencephaly
DI 23022.830: Myoclonic Epilepsy with Ragged Red Fibers Syndrome
DI 23022.836: Neurodegeneration with Brain Iron Accumulation- Type 1 and 2
DI 23022.845: Ohtahara Syndrome
DI 23022.850: Orthochromatic Leukodystrophy with Pigmented Glia
DI 23022.860: Pelizaeus-Merzbacher Disease--Classic Form
DI 23022.865: Pelizaeus-Merzbacher Disease--Connatal Form
DI 23022.875: Perry Syndrome
DI 23022.905: Stiff Person Syndrome
DI 23022.910: Tabes Dorsalis
DI 23022.923: Adult Onset Huntington Disease
DI 23022.925: Allan-Herndon-Dudley Syndrome
DI 23022.935: Caudal Regression Syndrome- Types III and IV
DI 23022.941: De Sanctis Cacchione Syndrome
DI 23022.949: Fatal Familial Insomnia
DI 23022.967: MECP2 Duplication Syndrome
DI 23022.973: Nonketotic Hyperglycinemia
DI 23022.977: Phelan-Mcdermid Syndrome
DI 23022.981: Roberts Syndrome
SI 00820.560: Allocating Work Expenses
NL 00703.474: Reconsideration Affirmation of Prior Decision