DI 23022.000 Processing Quick Disability Determination (QDD) and Compassionate Allowances (CAL) in the Disability Determination Services (DDS)

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DI 23022.010 Compassionate Allowances (CAL) and Quick Disability Determinations (QDD) Fast-Track Processes TN 24 02-19
DI 23022.020 Compassionate Allowances and Quick Disability Determinations Fast-Track Adjudicator Qualifications TN 24 02-19
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 24 02-19
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 50 11-21
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 47 08-21
DI 23022.085 Acute Leukemia TN 35 08-20
DI 23022.090 Adrenal Cancer TN 35 08-20
DI 23022.095 Alexander Disease TN 34 08-20
DI 23022.100 Amyotrophic Lateral Sclerosis (ALS) TN 35 08-20
DI 23022.105 Anaplastic Adrenal Cancer - Adult TN 35 08-20
DI 23022.106 Angiosarcoma TN 35 08-20
DI 23022.110 Astrocytoma - Grade III and IV TN 35 08-20
DI 23022.111 Atypical Teratoid/Rhabdoid Tumor TN 40 10-20
DI 23022.115 Bladder Cancer TN 35 08-20
DI 23022.120 Osteosarcoma TN 32 08-20
DI 23022.125 Breast Cancer – with distant metastases or recurrent TN 35 08-20
DI 23022.127 CACH - Vanishing White Matter Disease - Congenital, Infantile, and Early Childhood Onset Forms TN 34 08-20
DI 23022.130 Canavan Disease TN 34 08-20
DI 23022.133 CDKL5 Deficiency Disorder TN 35 08-20
DI 23022.135 Cerebro Oculo Facio Skeletal (COFS) Syndrome TN 35 08-20
DI 23022.136 Chronic Idiopathic Intestinal Pseudo Obstruction TN 35 08-20
DI 23022.140 Chronic Myelogenous Leukemia (CML) - Blast Phase TN 35 08-20
DI 23022.141 Coffin-Lowry Syndrome TN 34 08-20
DI 23022.143 Congenital Myotonic Dystrophy TN 34 08-20
DI 23022.144 Charlevoix-Saguenay Spastic Ataxia TN 46 08-21
DI 23022.145 Creutzfeldt-Jakob Disease (CJD) TN 51 12-21
DI 23022.146 Desmoplastic Small Round Cell Tumors TN 37 09-20
DI 23022.150 Ependymoblastoma (Child Brain Cancer) TN 35 08-20
DI 23022.155 Esophageal Cancer TN 35 08-20
DI 23022.156 Esthesioneuroblastoma TN 35 08-20
DI 23022.160 Farber's Disease TN 34 08-20
DI 23022.163 Fibrolamellar Cancer TN 35 08-20
DI 23022.165 Friedreich's Ataxia (FRDA) TN 34 08-20
DI 23022.170 Frontotemporal Dementia (FTD), Pick's Disease - Type A TN 34 08-20
DI 23022.175 Gallbladder Cancer TN 35 08-20
DI 23022.180 Gaucher Disease (GD) - Type 2 TN 35 08-20
DI 23022.181 Giant Axonal Neuropathy TN 34 08-20
DI 23022.185 Glioblastoma (Adult Brain Cancer) TN 35 08-20
DI 23022.186 GM1 - Gangliosidosis - Infantile & Juvenile Forms TN 28 08-20
DI 23022.190 Head and Neck Cancers TN 34 08-20
DI 23022.191 Hoyeraal-Hreidarsson Syndrome TN 34 08-20
DI 23022.195 Infantile Neuroaxonal Dystrophy (INAD) TN 34 08-20
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 34 08-20
DI 23022.205 Kidney Cancer TN 35 08-20
DI 23022.207 Kleefstra Syndrome TN 34 08-20
DI 23022.210 Krabbe Disease (KD) - Infantile TN 34 08-20
DI 23022.215 Large Intestine Cancer TN 35 08-20
DI 23022.216 Leptomeningeal Carcinomatosis TN 35 08-20
DI 23022.220 Lesch-Nyhan Syndrome (LNS) TN 34 08-20
DI 23022.221 Liposarcoma - Metastatic or Recurrent TN 35 08-20
DI 23022.225 Liver Cancer TN 35 08-20
DI 23022.226 Malignant Ectomesenchymoma TN 35 08-20
DI 23022.227 Malignant Renal Rhabdoid Tumor TN 35 08-20
DI 23022.230 Mantle Cell Lymphoma (MCL) TN 35 08-20
DI 23022.231 Marshall-Smith Syndrome TN 35 08-20
DI 23022.233 Megacystis Microcolon Intestinal Hypoperistalsis Syndrome TN 35 08-20
DI 23022.234 Megalencephaly-Capillary Malformation Syndrome TN 35 08-20
DI 23022.235 Metachromatic Leukodystrophy (MLD) TN 34 08-20
DI 23022.236 Nicolaides-Baraitser Syndrome TN 28 08-20
DI 23022.238 SYNGAP1-related NSID TN 45 08-21
DI 23022.240 Niemann-Pick Disease (NPD) - Type A TN 35 08-20
DI 23022.245 Non-Small Cell Lung Cancer TN 35 08-20
DI 23022.246 Oligodendroglioma Brain Cancer - Grade III TN 35 08-20
DI 23022.250 Ornithine Transcarbamylase (OTC) Deficiency TN 34 08-20
DI 23022.255 Osteogenesis Imperfecta (OI) - Type II TN 35 08-20
DI 23022.260 Ovarian Cancer TN 33 08-20
DI 23022.261 Pallister-Killian Syndrome TN 34 08-20
DI 23022.265 Pancreatic Cancer TN 33 08-20
DI 23022.266 Pericardial Mesothelioma TN 45 08-21
DI 23022.270 Peritoneal Mesothelioma TN 33 08-20
DI 23022.275 Pleural Mesothelioma TN 33 08-20
DI 23022.280 Pompe Disease - Infantile TN 34 08-20
DI 23022.281 Progressive Bulbar Palsy TN 34 08-20
DI 23022.282 Prostate Cancer – Hormone Refractory Disease – or with Visceral Metastases TN 33 08-20
DI 23022.283 Refractory Hodgkin Lymphoma TN 45 08-21
DI 23022.284 Renpenning Syndrome TN 45 08-21
DI 23022.285 Rett Syndrome (RTT) TN 34 08-20
DI 23022.286 Revesz Syndrome TN 33 08-20
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 Sjogren-Larsson Syndrome TN 34 08-20
DI 23022.298 Secondary Adenocarcinoma of the Brain TN 40 10-20
DI 23022.300 Small Cell Cancer of the Large Intestine TN 34 08-20
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 36 09-20
DI 23022.320 Small Cell Lung Cancer TN 36 09-20
DI 23022.325 Small Intestine Cancer TN 40 10-20
DI 23022.326 Soft Tissue Sarcoma - with Distant Metastases or Recurrent TN 36 09-20
DI 23022.330 Spinal Muscular Atrophy (SMA) - Types 0 and 1 TN 40 10-20
DI 23022.335 Stomach Cancer TN 36 09-20
DI 23022.337 Superficial Siderosis of the Central Nervous System TN 36 09-20
DI 23022.340 Anaplastic Thyroid Cancer TN 48 09-21
DI 23022.341 Taybi-Linder Syndrome TN 47 08-21
DI 23022.343 Tetrasomy 18p TN 36 09-20
DI 23022.345 Ureter Cancer TN 36 09-20
DI 23022.346 X-Linked Lymphoproliferative Disease TN 36 09-20
DI 23022.347 X-Linked Myotubular Myopathy TN 49 10-21
DI 23022.350 Alstrom Syndrome TN 31 08-20
DI 23022.355 Amegakaryocytic Thrombocytopenia TN 31 08-20
DI 23022.360 Ataxia Telangiectasia TN 38 09-20
DI 23022.365 Batten Disease TN 40 10-20
DI 23022.370 Bilateral Retinoblastoma TN 31 08-20
DI 23022.373 Congenital Zika Syndrome TN 47 08-21
DI 23022.375 Cri du Chat Syndrome TN 40 10-20
DI 23022.380 Degos Disease - Systemic TN 31 08-20
DI 23022.382 Desmoplastic Mesothelioma TN 45 08-21
DI 23022.385 Early-Onset Alzheimer's Disease TN 38 09-20
DI 23022.390 Edwards Syndrome (Trisomy 18) TN 41 10-20
DI 23022.395 Fibrodysplasia Ossificans Progressiva TN 49 10-21
DI 23022.400 Fukuyama Congenital Muscular Dystrophy TN 40 10-20
DI 23022.405 Hemophagocytic Lymphohistiocytosis TN 32 08-20
DI 23022.410 MPS II - Hunter Syndrome TN 35 08-20
DI 23022.415 MPS I - Hurler Syndrome TN 35 08-20
DI 23022.420 Idiopathic Pulmonary Fibrosis TN 35 08-20
DI 23022.425 Infantile Neuronal Ceroid-Lipofuscinoses TN 38 09-20
DI 23022.430 Junctional Epidermolysis Bullosa Lethal Type TN 35 08-20
DI 23022.435 Late Infantile Neuronal Ceroid-Lipofuscinoses TN 40 10-20
DI 23022.440 Leigh's Disease TN 35 08-20
DI 23022.445 Maple Syrup Urine Disease TN 38 09-20
DI 23022.450 Merosin Deficient Congenital Muscular Dystrophy TN 40 10-20
DI 23022.455 Mixed Dementias TN 38 09-20
DI 23022.460 Mucosal Malignant Melanoma TN 32 08-20
DI 23022.465 Neonatal Adrenoleukodystrophy TN 32 08-20
DI 23022.470 (Neonatal) Glutaric Acidemia TN 32 08-20
DI 23022.475 Niemann-Pick Disease - Type C TN 32 08-20
DI 23022.480 Patau Syndrome (Trisomy 13) TN 33 08-20
DI 23022.483 Primary Peritoneal Cancer TN 33 08-20
DI 23022.485 Primary Progressive Aphasia TN 33 08-20
DI 23022.490 Progressive Multifocal Leukoencephalopathy TN 40 10-20
DI 23022.495 MPS III - Sanfilippo Syndrome TN 35 08-20
DI 23022.496 SCN8A-related Epilepsy with Encephalopathy TN 45 08-21
DI 23022.500 Spinocerebellar Ataxia TN 36 09-20
DI 23022.505 Subacute Sclerosing Panencephalitis TN 40 10-20
DI 23022.510 Tay Sachs Disease, Infantile Type TN 36 09-20
DI 23022.515 Thanatophoric Dysplasia, Type 1 TN 36 09-20
DI 23022.520 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 23022.540 Aortic Atresia TN 31 08-20
DI 23022.543 CIC-rearranged Sarcoma TN 47 08-21
DI 23022.545 Eisenmenger Syndrome TN 31 08-20
DI 23022.550 Endomyocardial Fibrosis TN 31 08-20
DI 23022.555 Heart Transplant Graft Failure TN 32 08-20
DI 23022.560 Heart Transplant Wait List 1A/1B TN 32 08-20
DI 23022.565 Hypoplastic Left Heart Syndrome TN 32 08-20
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 31 08-20
DI 23022.585 Pulmonary Atresia TN 33 08-20
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 38 09-20
DI 23022.610 Lewy Body Dementia TN 38 09-20
DI 23022.615 Lowe Syndrome TN 35 08-20
DI 23022.620 Malignant Multiple Sclerosis TN 38 09-20
DI 23022.625 Multicentric Castleman Disease TN 38 09-20
DI 23022.630 Multiple System Atrophy TN 39 10-20
DI 23022.635 Paraneoplastic Pemphigus TN 33 08-20
DI 23022.640 Primary Central Nervous System Lymphoma TN 33 08-20
DI 23022.645 Primary Effusion Lymphoma TN 33 08-20
DI 23022.650 Progressive Supranuclear Palsy TN 33 08-20
DI 23022.655 Pulmonary Kaposi Sarcoma TN 33 08-20
DI 23022.660 The ALS Parkinsonism Dementia Complex TN 35 08-20
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 30 08-20
DI 23022.680 Alpha Mannosidosis--Type II and III TN 30 08-20
DI 23022.685 Carcinoma of Unknown Primary Site TN 35 08-20
DI 23022.690 Cerebrotendinous Xanthomatosis TN 30 08-20
DI 23022.695 Child Neuroblastoma—with distant metastases or recurrent TN 35 08-20
DI 23022.700 Child Lymphoma TN 35 08-20
DI 23022.705 Chondrosarcoma—with multimodal therapy TN 35 08-20
DI 23022.710 Cornelia de Lange Syndrome--Classic Form TN 35 08-20
DI 23022.715 Ewing Sarcoma TN 35 08-20
DI 23022.720 Follicular Dendritic Cell Sarcoma -- metastatic or recurrent TN 35 08-20
DI 23022.725 Fucosidosis -- Type I TN 35 08-20
DI 23022.730 Galactosialidosis -- Early and Late Infantile Types TN 35 08-20
DI 23022.735 Glioma - Grade III and IV TN 35 08-20
DI 23022.745 Hepatoblastoma TN 32 08-20
DI 23022.750 Histiocytosis Syndromes TN 32 08-20
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 32 08-20
DI 23022.775 I Cell Disease TN 32 08-20
DI 23022.780 Infantile Free Sialic Acid Storage Disease TN 32 08-20
DI 23022.785 Juvenile Onset Huntington Disease TN 30 08-20
DI 23022.790 Kufs Disease -- Type A and B TN 30 08-20
DI 23022.795 Lissencephaly TN 30 08-20
DI 23022.800 Lymphomatoid Granulomatosis -- Grade III TN 32 08-20
DI 23022.805 Malignant Brainstem Gliomas -- Childhood TN 32 08-20
DI 23022.810 Skin Malignant Melanoma with Metastases TN 33 08-20
DI 23022.815 Mastocytosis Type IV TN 32 08-20
DI 23022.820 Medulloblastoma TN 32 08-20
DI 23022.825 Merkel Cell Carcinoma – with metastases TN 32 08-20
DI 23022.830 Myoclonic Epilepsy with Ragged Red Fibers Syndrome TN 41 10-20
DI 23022.835 Nephrogenic Systemic Fibrosis TN 49 10-21
DI 23022.836 Neurodegeneration with Brain Iron Accumulation - Type 1 and 2 TN 30 08-20
DI 23022.840 Obliterative Bronchiolitis TN 32 08-20
DI 23022.845 Ohtahara Syndrome TN 30 08-20
DI 23022.850 Orthochromatic Leukodystrophy with Pigmented Glia TN 44 11-20
DI 23022.855 Pearson Syndrome TN 33 08-20
DI 23022.860 Pelizaeus-Merzbacher Disease--Classic Form TN 30 08-20
DI 23022.865 Pelizaeus-Merzbacher Disease--Connatal Form TN 30 08-20
DI 23022.870 Peripheral Nerve Cancer – metastatic or recurrent TN 33 08-20
DI 23022.875 Perry Syndrome TN 30 08-20
DI 23022.877 Pitt Hopkins Syndrome TN 33 08-20
DI 23022.880 Rhabdomyosarcoma TN 33 08-20
DI 23022.885 Rhizomelic Chondrodysplasia Punctata TN 33 08-20
DI 23022.887 Richter Syndrome TN 33 08-20
DI 23022.890 Schindler Disease -- Type I TN 33 08-20
DI 23022.895 Smith Lemli Opitz Syndrome TN 36 09-20
DI 23022.900 Spinal Nerve Root Cancer – metastatic or recurrent TN 36 09-20
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 36 09-20
DI 23022.921 Adult Non-Hodgkin Lymphoma TN 31 08-20
DI 23022.923 Adult Onset Huntington Disease TN 30 08-20
DI 23022.925 Allan-Herndon-Dudley Syndrome TN 30 08-20
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 31 08-20
DI 23022.933 Bilateral Optic Atrophy - Infantile TN 31 08-20
DI 23022.935 Caudal Regression Syndrome - Types III and IV TN 30 08-20
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 49 10-21
DI 23022.940 Duchenne Muscular Dystrophy - Adult TN 46 08-21
DI 23022.941 De Sanctis Cacchione Syndrome TN 30 08-20
DI 23022.943 Dravet Syndrome TN 31 08-20
DI 23022.945 Endometrial Stromal Sarcoma TN 31 08-20
DI 23022.947 Erdheim Chester Disease TN 41 10-20
DI 23022.949 Fatal Familial Insomnia TN 30 08-20
DI 23022.951 Fryns Syndrome TN 31 08-20
DI 23022.953 Fulminant Giant Cell Myocarditis TN 31 08-20
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 32 08-20
DI 23022.961 Leiomyosarcoma TN 32 08-20
DI 23022.963 Malignant Gastrointestinal Stromal Tumor TN 32 08-20
DI 23022.965 Malignant Germ Cell Tumor TN 32 08-20
DI 23022.967 MECP2 Duplication Syndrome TN 30 08-20
DI 23022.969 Menkes Disease - Classic or Infantile Onset Form TN 32 08-20
DI 23022.971 NFU-1 Mitochondrial Disease TN 32 08-20
DI 23022.973 Nonketotic Hyperglycinemia TN 30 08-20
DI 23022.975 Peritoneal Mucinous Carcinomatosis TN 33 08-20
DI 23022.977 Phelan-Mcdermid Syndrome TN 30 08-20
DI 23022.979 Retinopathy of Prematurity - Stage V 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

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DI 23022.000 - Processing Quick Disability Determination (QDD) and Compassionate Allowances (CAL) in the Disability Determination Services (DDS) - Table of Contents - 12/02/2021
Batch run: 12/02/2021
Rev:12/02/2021