| Section |  | Latest Transmittal
 | 
            
            
               | DI 23022.010 | Compassionate Allowances (CAL) and Quick Disability Determinations (QDD) Fast-Track
                  Processes | TN 56 05-23 | 
            
            
               | DI 23022.030 | Identifying and Receipting Compassionate Allowances (CAL) and Quick Disability Determinations
                  (QDD) Cases | TN 24 02-19 | 
            
            
               | DI 23022.040 | Compassionate Allowances (CAL) and Quick Disability Determinations (QDD) Fast-Track
                  Case Development | TN 56 05-23 | 
            
            
               | DI 23022.050 | Making the Determination in Compassionate Allowances (CAL) or Quick Disability Determinations
                  (QDD) Fast-Track Cases | TN 18 11-18 | 
            
            
               | DI 23022.055 | Adding and Modifying Compassionate Allowances (CAL) Status; Removing and Reinstating
                  CAL and Quick Disability Determinations (QDD) Status | TN 71 07-24 | 
            
            
               | DI 23022.060 | Disability Determination Services Jurisdiction When a Compassionate Allowances or
                  Quick Disability Determinations Claimant Moves to another State or Leaves the United
                  States | TN 24 02-19 | 
            
            
               | DI 23022.075 | Appeals Processing of Compassionate Allowances (CAL) Cases | TN 24 02-19 | 
            
            
               | DI 23022.080 | List of Compassionate Allowances (CAL) Conditions | TN 79 08-25 | 
            
            
               | DI 23022.081 | 1p36 Deletion Syndrome | TN 81 09-25 | 
            
            
               | DI 23022.082 | Adult Heart Transplant Wait List – Status Levels 1-4 | TN 73 08-24 | 
            
            
               | DI 23022.085 | Acute Leukemia | TN 35 08-20 | 
            
            
               | DI 23022.090 | Adrenal Cancer with Distant Metastases or Inoperable, Unresectable or Recurrent | TN 82 09-25 | 
            
            
               | DI 23022.095 | Alexander Disease - Neonatal and Infantile | TN 80 08-25 | 
            
            
               | DI 23022.100 | Amyotrophic Lateral Sclerosis (ALS) - ADULT | TN 69 12-23 | 
            
            
               | DI 23022.105 | Anaplastic Adrenal Cancer - Adult with Distant Metastases or Inoperable, Unresectable
                  or Recurrent | TN 61 10-23 | 
            
            
               | DI 23022.106 | Angiosarcoma | TN 54 09-22 | 
            
            
               | DI 23022.110 | Astrocytoma – Grade III and IV | TN 81 09-25 | 
            
            
               | DI 23022.111 | Atypical Teratoid/Rhabdoid Tumor | TN 81 09-25 | 
            
            
               | DI 23022.112 | Bainbridge-Ropers Syndrome | TN 73 08-24 | 
            
            
               | DI 23022.113 | Bilateral Anophthalmia | TN 79 08-25 | 
            
            
               | DI 23022.115 | Bladder Cancer with Distant Metastases or Inoperable or Unresectable | TN 81 09-25 | 
            
            
               | DI 23022.117 | Blastic Plasmacytoid Dendritic Cell Neoplasm | TN 81 09-25 | 
            
            
               | DI 23022.120 | Osteosarcoma, Formerly Known As Bone Cancer | TN 85 09-25 | 
            
            
               | DI 23022.125 | Breast Cancer – with Distant Metastases or Recurrent | TN 81 09-25 | 
            
            
               | DI 23022.127 | CACH - Vanishing White Matter Disease - Congenital, Infantile, and Early Childhood
                  Onset Forms | TN 81 09-25 | 
            
            
               | DI 23022.128 | Calciphylaxis | TN 57 08-23 | 
            
            
               | DI 23022.130 | Canavan Disease | TN 81 09-25 | 
            
            
               | DI 23022.131 | Carey-Fineman-Ziter Syndrome | TN 79 08-25 | 
            
            
               | DI 23022.133 | CDKL5 Deficiency Disorder | TN 81 09-25 | 
            
            
               | DI 23022.135 | Cerebro Oculo Facio Skeletal (COFS) Syndrome | TN 35 08-20 | 
            
            
               | DI 23022.136 | Chronic Idiopathic Intestinal Pseudo Obstruction | TN 54 09-22 | 
            
            
               | DI 23022.140 | Chronic Myelogenous Leukemia (CML) – Blast Phase | TN 81 09-25 | 
            
            
               | DI 23022.141 | Coffin-Lowry Syndrome | TN 34 08-20 | 
            
            
               | DI 23022.143 | Congenital Myotonic Dystrophy | TN 82 09-25 | 
            
            
               | DI 23022.144 | Charlevoix-Saguenay Spastic Ataxia | TN 81 09-25 | 
            
            
               | DI 23022.145 | Creutzfeldt-Jakob Disease (CJD) - Adult | TN 82 09-25 | 
            
            
               | DI 23022.146 | Desmoplastic Small Round Cell Tumors | TN 82 09-25 | 
            
            
               | DI 23022.150 | Ependymoblastoma (Child Brain Cancer) | TN 82 09-25 | 
            
            
               | DI 23022.155 | Esophageal Cancer | TN 82 09-25 | 
            
            
               | DI 23022.156 | Esthesioneuroblastoma | TN 82 09-25 | 
            
            
               | DI 23022.160 | Farber Disease - Infantile | TN 81 09-25 | 
            
            
               | DI 23022.163 | Fibrolamellar Cancer | TN 82 09-25 | 
            
            
               | DI 23022.165 | Friedreich's Ataxia (FRDA) | TN 82 09-25 | 
            
            
               | DI 23022.170 | Frontotemporal Dementia (FTD), Pick's Disease - Type A - Adult | TN 82 09-25 | 
            
            
               | DI 23022.175 | Gallbladder Cancer | TN 35 08-20 | 
            
            
               | DI 23022.180 | Gaucher Disease (GD) - Type 2 | TN 82 09-25 | 
            
            
               | DI 23022.181 | Giant Axonal Neuropathy | TN 34 08-20 | 
            
            
               | DI 23022.185 | Glioblastoma Multiforme (Adult Brain Cancer) | TN 82 09-25 | 
            
            
               | DI 23022.186 | GM1 - Gangliosidosis - Infantile and Juvenile Forms | TN 82 09-25 | 
            
            
               | DI 23022.188 | Harlequin Ichthyosis - Child | TN 79 08-25 | 
            
            
               | DI 23022.190 | Head and Neck Cancers - with Distant Metastasis or Inoperable or Unresectable | TN 82 09-25 | 
            
            
               | DI 23022.191 | Hoyeraal-Hreidarsson Syndrome | TN 82 09-25 | 
            
            
               | DI 23022.195 | Infantile Neuroaxonal Dystrophy (INAD) | TN 83 09-25 | 
            
            
               | DI 23022.200 | Inflammatory Breast Cancer | TN 35 08-20 | 
            
            
               | DI 23022.201 | Intracranial Hemangiopericytoma | TN 35 08-20 | 
            
            
               | DI 23022.202 | Joubert Syndrome | TN 83 09-25 | 
            
            
               | DI 23022.205 | Kidney Cancer - Inoperable or Unresectable | TN 83 09-25 | 
            
            
               | DI 23022.207 | Kleefstra Syndrome | TN 83 09-25 | 
            
            
               | DI 23022.210 | Krabbe Disease (KD) - Infantile | TN 83 09-25 | 
            
            
               | DI 23022.215 | Large Intestine Cancer - with Distant Metastasis or Inoperable, Unresectable or Recurrent | TN 83 09-25 | 
            
            
               | DI 23022.216 | Leptomeningeal Carcinomatosis | TN 83 09-25 | 
            
            
               | DI 23022.220 | Lesch-Nyhan Syndrome (LNS) | TN 83 09-25 | 
            
            
               | DI 23022.221 | Liposarcoma - Metastatic or Recurrent | TN 54 09-22 | 
            
            
               | DI 23022.223 | LMNA-related Congenital Muscular Dystrophy | TN 79 08-25 | 
            
            
               | DI 23022.225 | Hepatocellular Carcinoma | TN 82 09-25 | 
            
            
               | DI 23022.226 | Malignant Ectomesenchymoma | TN 83 09-25 | 
            
            
               | DI 23022.227 | Malignant Renal Rhabdoid Tumor | TN 35 08-20 | 
            
            
               | DI 23022.230 | Mantle Cell Lymphoma (MCL) | TN 83 09-25 | 
            
            
               | DI 23022.231 | Marshall-Smith Syndrome | TN 35 08-20 | 
            
            
               | DI 23022.233 | Megacystis Microcolon Intestinal Hypoperistalsis Syndrome | TN 84 09-25 | 
            
            
               | DI 23022.234 | Megalencephaly-Capillary Malformation Syndrome | TN 84 09-25 | 
            
            
               | DI 23022.235 | Metachromatic Leukodystrophy (MLD) - Late Infantile | TN 84 09-25 | 
            
            
               | DI 23022.236 | Nicolaides-Baraitser Syndrome | TN 84 09-25 | 
            
            
               | DI 23022.238 | SYNGAP1-related NSID | TN 45 08-21 | 
            
            
               | DI 23022.240 | Niemann-Pick Disease (NPD) - Type A | TN 84 09-25 | 
            
            
               | DI 23022.245 | Non-Small Cell Lung Cancer | TN 85 09-25 | 
            
            
               | DI 23022.246 | Oligodendroglioma Brain Cancer - Grade III | TN 85 09-25 | 
            
            
               | DI 23022.250 | Ornithine Transcarbamylase (OTC) Deficiency | TN 85 09-25 | 
            
            
               | DI 23022.255 | Osteogenesis Imperfecta (OI) - Type II | TN 85 09-25 | 
            
            
               | DI 23022.260 | Ovarian Cancer - with Distant Metastases or Inoperable or Unresectable | TN 60 10-23 | 
            
            
               | DI 23022.261 | Pallister-Killian Syndrome | TN 85 09-25 | 
            
            
               | DI 23022.265 | Pancreatic Cancer | TN 85 09-25 | 
            
            
               | DI 23022.266 | Pericardial Mesothelioma | TN 85 09-25 | 
            
            
               | DI 23022.270 | Peritoneal Mesothelioma | TN 85 09-25 | 
            
            
               | DI 23022.273 | Pineoblastoma – Childhood | TN 85 09-25 | 
            
            
               | DI 23022.274 | Plasmablastic Lymphoma | TN 73 08-24 | 
            
            
               | DI 23022.275 | Pleural Mesothelioma | TN 85 09-25 | 
            
            
               | DI 23022.280 | Pompe Disease – Infantile | TN 85 09-25 | 
            
            
               | DI 23022.281 | Progressive Bulbar Palsy | TN 34 08-20 | 
            
            
               | DI 23022.282 | Prostate Cancer – Hormone Refractory Disease – or with Visceral Metastases | TN 60 10-23 | 
            
            
               | DI 23022.283 | Refractory Hodgkin Lymphoma | TN 45 08-21 | 
            
            
               | DI 23022.284 | Renpenning Syndrome | TN 54 09-22 | 
            
            
               | DI 23022.285 | Rett Syndrome (RTT) | TN 34 08-20 | 
            
            
               | DI 23022.286 | Revesz Syndrome | TN 54 09-22 | 
            
            
               | DI 23022.287 | Rubinstein-Taybi Syndrome | TN 28 08-20 | 
            
            
               | DI 23022.290 | Salivary Cancers | TN 33 08-20 | 
            
            
               | DI 23022.295 | Sandhoff Disease | TN 33 08-20 | 
            
            
               | DI 23022.296 | Seckel Syndrome | TN 34 08-20 | 
            
            
               | DI 23022.297 | Sjögren-Larsson Syndrome | TN 64 10-23 | 
            
            
               | DI 23022.298 | Secondary Adenocarcinoma of the Brain | TN 40 10-20 | 
            
            
               | DI 23022.300 | Small Cell Cancer of the Large Intestine | TN 54 09-22 | 
            
            
               | DI 23022.305 | Small Cell Cancer of the Ovary | TN 36 09-20 | 
            
            
               | DI 23022.310 | Small Cell Cancer of the Prostate | TN 36 09-20 | 
            
            
               | DI 23022.311 | Small Cell Cancer of the Thymus | TN 36 09-20 | 
            
            
               | DI 23022.315 | Small-Cell Cancer of the Female Genital Tract | TN 60 10-23 | 
            
            
               | DI 23022.320 | Small Cell Lung Cancer | TN 36 09-20 | 
            
            
               | DI 23022.325 | Small Intestine Cancer - with Distant Metastases or Inoperable or Recurrent | TN 60 10-23 | 
            
            
               | DI 23022.326 | Soft Tissue Sarcoma - with Distant Metastases or Recurrent | TN 60 10-23 | 
            
            
               | DI 23022.330 | Spinal Muscular Atrophy (SMA) - Types 0 and 1 | TN 40 10-20 | 
            
            
               | DI 23022.335 | Stomach Cancer, with Distant Metastases or Inoperable, Unresectable or Recurrent | TN 60 10-23 | 
            
            
               | DI 23022.337 | Superficial Siderosis of the Central Nervous System | TN 36 09-20 | 
            
            
               | DI 23022.340 | Anaplastic Thyroid Cancer | TN 60 10-23 | 
            
            
               | DI 23022.341 | Taybi-Linder Syndrome | TN 47 08-21 | 
            
            
               | DI 23022.343 | Tetrasomy 18p | TN 36 09-20 | 
            
            
               | DI 23022.344 | Trisomy 9 | TN 57 08-23 | 
            
            
               | DI 23022.345 | Ureter Cancer - with Metastases or Inoperable, Unresectable or Recurrent | TN 60 10-23 | 
            
            
               | DI 23022.346 | X-Linked Lymphoproliferative Disease | TN 36 09-20 | 
            
            
               | DI 23022.347 | X-Linked Myotubular Myopathy | TN 49 10-21 | 
            
            
               | DI 23022.349 | Zhu-Tokita-Takenouchi-Kim Syndrome | TN 79 08-25 | 
            
            
               | DI 23022.350 | Alstrom Syndrome | TN 81 09-25 | 
            
            
               | DI 23022.355 | Amegakaryocytic Thrombocytopenia | TN 81 09-25 | 
            
            
               | DI 23022.357 | Angioimmunoblastic T-Cell Lymphoma | TN 53 08-22 | 
            
            
               | DI 23022.360 | Ataxia Telangiectasia | TN 81 09-25 | 
            
            
               | DI 23022.363 | Au-Kline Syndrome | TN 79 08-25 | 
            
            
               | DI 23022.365 | Batten Disease | TN 81 09-25 | 
            
            
               | DI 23022.370 | Bilateral Retinoblastoma | TN 81 09-25 | 
            
            
               | DI 23022.373 | Congenital Zika Syndrome | TN 82 09-25 | 
            
            
               | DI 23022.374 | Costello Syndrome | TN 73 08-24 | 
            
            
               | DI 23022.375 | Cri du Chat Syndrome | TN 82 09-25 | 
            
            
               | DI 23022.380 | Degos Disease - Systemic | TN 82 09-25 | 
            
            
               | DI 23022.382 | Desmoplastic Mesothelioma | TN 45 08-21 | 
            
            
               | DI 23022.385 | Early-Onset Alzheimer's Disease | TN 78 03-25 | 
            
            
               | DI 23022.390 | Edwards Syndrome (Trisomy 18) | TN 69 12-23 | 
            
            
               | DI 23022.395 | Fibrodysplasia Ossificans Progressiva | TN 82 09-25 | 
            
            
               | DI 23022.400 | Fukuyama Congenital Muscular Dystrophy | TN 82 09-25 | 
            
            
               | DI 23022.403 | Gerstmann-Straussler-Scheinker Disease | TN 82 09-25 | 
            
            
               | DI 23022.404 | Hematopoietic Stem Cell Transplantation | TN 79 08-25 | 
            
            
               | DI 23022.405 | Hemophagocytic Lymphohistiocytosis - Familial Type (FHLH) | TN 82 09-25 | 
            
            
               | DI 23022.407 | Histiocytic Malignancies | TN 82 09-25 | 
            
            
               | DI 23022.410 | MPS II | TN 84 09-25 | 
            
            
               | DI 23022.415 | MPS I | TN 84 09-25 | 
            
            
               | DI 23022.420 | Idiopathic Pulmonary Fibrosis | TN 83 09-25 | 
            
            
               | DI 23022.425 | Infantile Neuronal Ceroid Lipofuscinoses | TN 83 09-25 | 
            
            
               | DI 23022.430 | Junctional Epidermolysis Bullosa - Lethal Type | TN 68 12-23 | 
            
            
               | DI 23022.435 | Late Infantile Neuronal Ceroid Lipofuscinoses | TN 83 09-25 | 
            
            
               | DI 23022.437 | Leber Congenital Amaurosis | TN 57 08-23 | 
            
            
               | DI 23022.440 | Leigh's Disease | TN 83 09-25 | 
            
            
               | DI 23022.445 | Maple Syrup Urine Disease | TN 83 09-25 | 
            
            
               | DI 23022.450 | Merosin Deficient Congenital Muscular Dystrophy | TN 84 09-25 | 
            
            
               | DI 23022.453 | Microvillus Inclusion Disease – Child | TN 84 09-25 | 
            
            
               | DI 23022.455 | Mixed Dementias | TN 84 09-25 | 
            
            
               | DI 23022.457 | Mowat-Wilson Syndrome | TN 53 08-22 | 
            
            
               | DI 23022.460 | Mucosal Malignant Melanoma | TN 84 09-25 | 
            
            
               | DI 23022.463 | Myelodysplastic Syndrome with Excess Blasts | TN 84 09-25 | 
            
            
               | DI 23022.465 | Neonatal Adrenoleukodystrophy | TN 84 09-25 | 
            
            
               | DI 23022.468 | Neonatal Marfan Syndrome | TN 84 09-25 | 
            
            
               | DI 23022.470 | Glutaric Acidemia - Type II | TN 61 10-23 | 
            
            
               | DI 23022.475 | Niemann-Pick Disease - Type C | TN 85 09-25 | 
            
            
               | DI 23022.477 | NUT Carcinoma | TN 85 09-25 | 
            
            
               | DI 23022.480 | Patau Syndrome (Trisomy 13) | TN 85 09-25 | 
            
            
               | DI 23022.481 | Pfeiffer Syndrome - Types II and III | TN 53 08-22 | 
            
            
               | DI 23022.482 | Pontocerebellar Hypoplasia | TN 85 09-25 | 
            
            
               | DI 23022.483 | Primary Peritoneal Cancer | TN 33 08-20 | 
            
            
               | DI 23022.485 | Primary Progressive Aphasia | TN 54 09-22 | 
            
            
               | DI 23022.490 | Progressive Multifocal Leukoencephalopathy | TN 40 10-20 | 
            
            
               | DI 23022.491 | Progressive Muscular Atrophy | TN 79 08-25 | 
            
            
               | DI 23022.492 | Pulmonary Amyloidosis – AL Type | TN 79 08-25 | 
            
            
               | DI 23022.493 | Rasmussen Encephalitis | TN 79 08-25 | 
            
            
               | DI 23022.495 | MPS III | TN 69 12-23 | 
            
            
               | DI 23022.496 | SCN8A-related Epilepsy with Encephalopathy | TN 45 08-21 | 
            
            
               | DI 23022.500 | Spinocerebellar Ataxia | TN 36 09-20 | 
            
            
               | DI 23022.503 | Snijders Blok-Campeau Syndrome | TN 73 08-24 | 
            
            
               | DI 23022.505 | Subacute Sclerosing Panencephalitis | TN 54 09-22 | 
            
            
               | DI 23022.510 | Tay Sachs Disease, Infantile Type | TN 36 09-20 | 
            
            
               | DI 23022.515 | Thanatophoric Dysplasia, Type 1 | TN 36 09-20 | 
            
            
               | DI 23022.516 | Thymic Carcinoma | TN 79 08-25 | 
            
            
               | DI 23022.518 | Turnpenny-Fry Syndrome | TN 79 08-25 | 
            
            
               | DI 23022.520 | Ullrich Congenital Muscular Dystrophy | TN 38 09-20 | 
            
            
               | DI 23022.525 | Walker Warburg Syndrome | TN 36 09-20 | 
            
            
               | DI 23022.530 | Wolman Disease | TN 36 09-20 | 
            
            
               | DI 23022.535 | Zellweger Syndrome | TN 36 09-20 | 
            
            
               | DI 23022.536 | Anaplastic Ependymoma | TN 81 09-25 | 
            
            
               | DI 23022.537 | WHO Grade III Meningiomas | TN 79 08-25 | 
            
            
               | DI 23022.540 | Aortic Atresia | TN 31 08-20 | 
            
            
               | DI 23022.543 | CIC-Rearranged Sarcoma | TN 82 09-25 | 
            
            
               | DI 23022.545 | Eisenmenger Syndrome | TN 82 09-25 | 
            
            
               | DI 23022.550 | Endomyocardial Fibrosis | TN 82 09-25 | 
            
            
               | DI 23022.555 | Heart Transplant Graft Failure | TN 82 09-25 | 
            
            
               | DI 23022.560 | Child Heart Transplant Wait List - Status Levels 1A/1B | TN 73 08-24 | 
            
            
               | DI 23022.565 | Hypoplastic Left Heart Syndrome | TN 82 09-25 | 
            
            
               | DI 23022.570 | Ventricular Assist Device Recipient — Left, Right, or Biventricular | TN 36 09-20 | 
            
            
               | DI 23022.575 | Mitral Valve Atresia | TN 32 08-20 | 
            
            
               | DI 23022.580 | Cardiac Amyloidosis - AL Type | TN 81 09-25 | 
            
            
               | DI 23022.585 | Pulmonary Atresia | TN 33 08-20 | 
            
            
               | DI 23022.586 | Sarcomatoid Carcinoma of the Lung—Stages II-IV | TN 57 08-23 | 
            
            
               | DI 23022.587 | Sarcomatoid Mesothelioma | TN 53 08-22 | 
            
            
               | DI 23022.590 | Single Ventricle | TN 33 08-20 | 
            
            
               | DI 23022.595 | Tricuspid Atresia | TN 36 09-20 | 
            
            
               | DI 23022.600 | Angelman Syndrome | TN 38 09-20 | 
            
            
               | DI 23022.605 | Corticobasal Degeneration | TN 82 09-25 | 
            
            
               | DI 23022.610 | Lewy Body Dementia | TN 83 09-25 | 
            
            
               | DI 23022.615 | Lowe Syndrome | TN 83 09-25 | 
            
            
               | DI 23022.620 | Malignant Multiple Sclerosis | TN 83 09-25 | 
            
            
               | DI 23022.625 | Multicentric Castleman Disease | TN 84 09-25 | 
            
            
               | DI 23022.630 | Multiple System Atrophy | TN 84 09-25 | 
            
            
               | DI 23022.633 | Paraneoplastic Cerebellar Degeneration | TN 57 08-23 | 
            
            
               | DI 23022.635 | Paraneoplastic Pemphigus | TN 62 10-23 | 
            
            
               | DI 23022.640 | Primary Central Nervous System Lymphoma | TN 85 09-25 | 
            
            
               | DI 23022.643 | Posterior Cortical Atrophy | TN 85 09-25 | 
            
            
               | DI 23022.645 | Primary Effusion Lymphoma | TN 33 08-20 | 
            
            
               | DI 23022.647 | Primary Omental Cancer | TN 57 08-23 | 
            
            
               | DI 23022.650 | Progressive Supranuclear Palsy | TN 33 08-20 | 
            
            
               | DI 23022.655 | Pulmonary Kaposi Sarcoma | TN 54 09-22 | 
            
            
               | DI 23022.660 | ALS/Parkinsonism Dementia Complex | TN 81 09-25 | 
            
            
               | DI 23022.665 | Aicardi--Goutieres Syndrome | TN 30 08-20 | 
            
            
               | DI 23022.670 | Alobar Holoprosencephaly | TN 43 10-20 | 
            
            
               | DI 23022.675 | Alpers Disease | TN 81 09-25 | 
            
            
               | DI 23022.680 | Alpha Mannosidosis – Types II and III | TN 81 09-25 | 
            
            
               | DI 23022.685 | Carcinoma of Unknown Primary Site | TN 35 08-20 | 
            
            
               | DI 23022.690 | Cerebrotendinous Xanthomatosis | TN 81 09-25 | 
            
            
               | DI 23022.695 | Child Neuroblastoma—with Distant Metastases or Recurrent | TN 81 09-25 | 
            
            
               | DI 23022.700 | Child Lymphoma | TN 81 09-25 | 
            
            
               | DI 23022.704 | Cholangiocarcinoma | TN 57 08-23 | 
            
            
               | DI 23022.705 | Chondrosarcoma—with multimodal therapy | TN 35 08-20 | 
            
            
               | DI 23022.710 | Cornelia de Lange Syndrome--Classic Form | TN 82 09-25 | 
            
            
               | DI 23022.715 | Ewing Sarcoma | TN 82 09-25 | 
            
            
               | DI 23022.720 | Follicular Dendritic Cell Sarcoma -- Metastatic or Recurrent | TN 82 09-25 | 
            
            
               | DI 23022.723 | FOXG1 Syndrome | TN 82 09-25 | 
            
            
               | DI 23022.725 | Fucosidosis -- Type I | TN 35 08-20 | 
            
            
               | DI 23022.730 | Galactosialidosis -- Early and Late Infantile Types | TN 82 09-25 | 
            
            
               | DI 23022.735 | Glioma - Grade III and IV | TN 82 09-25 | 
            
            
               | DI 23022.745 | Hepatoblastoma | TN 32 08-20 | 
            
            
               | DI 23022.750 | Histiocytosis Syndromes | TN 82 09-25 | 
            
            
               | DI 23022.755 | Hutchinson-Gilford Progeria Syndrome | TN 32 08-20 | 
            
            
               | DI 23022.760 | Hydranencephaly | TN 32 08-20 | 
            
            
               | DI 23022.765 | Hypocomplementemic Urticarial Vasculitis Syndrome | TN 43 10-20 | 
            
            
               | DI 23022.770 | Hypophosphatasia--Perinatal (Lethal) and Infantile Onset Types | TN 82 09-25 | 
            
            
               | DI 23022.775 | I Cell Disease | TN 82 09-25 | 
            
            
               | DI 23022.780 | Infantile Free Sialic Acid Storage Disease | TN 83 09-25 | 
            
            
               | DI 23022.785 | Juvenile Onset Huntington Disease | TN 83 09-25 | 
            
            
               | DI 23022.790 | Kufs Disease -- Type A and B | TN 83 09-25 | 
            
            
               | DI 23022.795 | Lissencephaly | TN 83 09-25 | 
            
            
               | DI 23022.800 | Lymphomatoid Granulomatosis -- Grade III | TN 83 09-25 | 
            
            
               | DI 23022.805 | Malignant Brainstem Gliomas -- Childhood | TN 83 09-25 | 
            
            
               | DI 23022.810 | Skin Malignant Melanoma with Metastases | TN 60 10-23 | 
            
            
               | DI 23022.815 | Mastocytosis Type IV | TN 84 09-25 | 
            
            
               | DI 23022.820 | Child Medulloblastoma | TN 84 09-25 | 
            
            
               | DI 23022.825 | Merkel Cell Carcinoma – with Metastases | TN 84 09-25 | 
            
            
               | DI 23022.827 | Metastatic Endometrial Adenocarcinoma | TN 84 09-25 | 
            
            
               | DI 23022.830 | Myoclonic Epilepsy with Ragged Red Fibers Syndrome | TN 84 09-25 | 
            
            
               | DI 23022.835 | Nephrogenic Systemic Fibrosis | TN 62 10-23 | 
            
            
               | DI 23022.836 | Neurodegeneration with Brain Iron Accumulation – Types 1 and 2 | TN 84 09-25 | 
            
            
               | DI 23022.840 | Obliterative Bronchiolitis | TN 85 09-25 | 
            
            
               | DI 23022.845 | Ohtahara Syndrome | TN 85 09-25 | 
            
            
               | DI 23022.850 | Orthochromatic Leukodystrophy with Pigmented Glia | TN 85 09-25 | 
            
            
               | DI 23022.853 | PACS1 Syndrome | TN 73 08-24 | 
            
            
               | DI 23022.855 | Pearson Syndrome | TN 85 09-25 | 
            
            
               | DI 23022.860 | Pelizaeus-Merzbacher Disease – Classic Form | TN 85 09-25 | 
            
            
               | DI 23022.865 | Pelizaeus-Merzbacher Disease – Connatal Form | TN 85 09-25 | 
            
            
               | DI 23022.870 | Peripheral Nerve Cancer – Metastatic or Recurrent | TN 85 09-25 | 
            
            
               | DI 23022.875 | Perry Syndrome | TN 30 08-20 | 
            
            
               | DI 23022.877 | Pitt Hopkins Syndrome | TN 85 09-25 | 
            
            
               | DI 23022.878 | Renal Amyloidosis – AL Type | TN 53 08-22 | 
            
            
               | DI 23022.879 | Renal Medullary Carcinoma | TN 73 08-24 | 
            
            
               | DI 23022.880 | Rhabdomyosarcoma | TN 33 08-20 | 
            
            
               | DI 23022.885 | Rhizomelic Chondrodysplasia Punctata | TN 33 08-20 | 
            
            
               | DI 23022.887 | Richter Syndrome | TN 54 09-22 | 
            
            
               | DI 23022.890 | Schindler Disease -- Type I | TN 69 12-23 | 
            
            
               | DI 23022.895 | Smith Lemli Opitz Syndrome | TN 36 09-20 | 
            
            
               | DI 23022.900 | Spinal Nerve Root Cancer – Metastatic or Recurrent | TN 60 10-23 | 
            
            
               | DI 23022.905 | Stiff Person Syndrome | TN 30 08-20 | 
            
            
               | DI 23022.910 | Tabes Dorsalis | TN 30 08-20 | 
            
            
               | DI 23022.915 | Wolf-Hirschhorn Syndrome | TN 36 09-20 | 
            
            
               | DI 23022.920 | Xeroderma Pigmentosum | TN 62 10-23 | 
            
            
               | DI 23022.921 | Adult Non-Hodgkin Lymphoma | TN 81 09-25 | 
            
            
               | DI 23022.923 | Adult Onset Huntington Disease | TN 81 09-25 | 
            
            
               | DI 23022.925 | Allan-Herndon-Dudley Syndrome | TN 81 09-25 | 
            
            
               | DI 23022.927 | Alveolar Soft Part Sarcoma | TN 31 08-20 | 
            
            
               | DI 23022.929 | Aplastic Anemia | TN 31 08-20 | 
            
            
               | DI 23022.931 | Beta Thalassemia Major | TN 75 12-24 | 
            
            
               | DI 23022.933 | Bilateral Optic Atrophy – Infantile | TN 81 09-25 | 
            
            
               | DI 23022.935 | Caudal Regression Syndrome - Types III and IV | TN 81 09-25 | 
            
            
               | DI 23022.937 | Child Lymphoblastic Lymphoma | TN 41 10-20 | 
            
            
               | DI 23022.938 | Choroid Plexus Carcinoma | TN 45 08-21 | 
            
            
               | DI 23022.939 | Congenital Lymphedema | TN 82 09-25 | 
            
            
               | DI 23022.940 | Duchenne Muscular Dystrophy - Adult | TN 46 08-21 | 
            
            
               | DI 23022.941 | De Sanctis Cacchione Syndrome | TN 62 10-23 | 
            
            
               | DI 23022.943 | Dravet Syndrome | TN 82 09-25 | 
            
            
               | DI 23022.945 | Endometrial Stromal Sarcoma | TN 82 09-25 | 
            
            
               | DI 23022.947 | Erdheim Chester Disease | TN 41 10-20 | 
            
            
               | DI 23022.949 | Fatal Familial Insomnia | TN 82 09-25 | 
            
            
               | DI 23022.951 | Fryns Syndrome | TN 82 09-25 | 
            
            
               | DI 23022.953 | Fulminant Giant Cell Myocarditis | TN 82 09-25 | 
            
            
               | DI 23022.955 | Hepatopulmonary Syndrome | TN 32 08-20 | 
            
            
               | DI 23022.957 | Hepatorenal Syndrome | TN 32 08-20 | 
            
            
               | DI 23022.959 | Jervell and Lange-Nielsen Syndrome | TN 83 09-25 | 
            
            
               | DI 23022.961 | Leiomyosarcoma | TN 83 09-25 | 
            
            
               | DI 23022.963 | Malignant Gastrointestinal Stromal Tumor | TN 32 08-20 | 
            
            
               | DI 23022.965 | Malignant Germ Cell Tumor | TN 83 09-25 | 
            
            
               | DI 23022.967 | MECP2 Duplication Syndrome | TN 84 09-25 | 
            
            
               | DI 23022.969 | Menkes Disease - Classic or Infantile Onset Form | TN 84 09-25 | 
            
            
               | DI 23022.971 | NFU-1 Mitochondrial Disease | TN 84 09-25 | 
            
            
               | DI 23022.973 | Nonketotic Hyperglycinemia | TN 85 09-25 | 
            
            
               | DI 23022.975 | Peritoneal Mucinous Carcinomatosis | TN 85 09-25 | 
            
            
               | DI 23022.977 | Phelan-McDermid Syndrome | TN 85 09-25 | 
            
            
               | DI 23022.979 | Retinopathy of Prematurity - Stage V, Bilateral | TN 33 08-20 | 
            
            
               | DI 23022.981 | Roberts Syndrome | TN 49 10-21 | 
            
            
               | DI 23022.983 | Severe Combined Immunodeficiency -- Childhood | TN 33 08-20 | 
            
            
               | DI 23022.985 | Sinonasal Cancer | TN 33 08-20 | 
            
            
               | DI 23022.987 | Transplant Coronary Artery Vasculopathy | TN 36 09-20 | 
            
            
               | DI 23022.989 | Usher Syndrome - Type I | TN 36 09-20 |