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

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DI 23022.010Compassionate Allowances and Quick Disability Determinations Fast-Track ProcessesTN 9 06-13
DI 23022.020Compassionate Allowances and Quick Disability Determinations Fast-Track Adjudicator QualificationsTN 9 06-13
DI 23022.030Identifying and Receipting Compassionate Allowances and Quick Disability Determinations CasesTN 9 06-13
DI 23022.040Compassionate Allowances and Quick Disability Determinations Fast-Track Case DevelopmentTN 9 06-13
DI 23022.050Making the Determination in a Compassionate Allowances or Quick Disability Determinations Fast-Track CasesTN 9 06-13
DI 23022.053Coding for All Compassionate Allowances and Quick Disability Determinations Fast-Track CasesTN 9 06-13
DI 23022.055Actions on Compassionate Allowances and Disability Determinations Fast-Track CasesTN 9 06-13
DI 23022.060Disability Determination Services Jurisdiction When a Compassionate Allowance or Quick Disability Determination Claimant Moves to another State or Leaves the United StatesTN 9 06-13
DI 23022.075Appeals Processing of Compassionate Allowances CasesTN 9 06-13
DI 23022.080List of Compassionate Allowance (CAL) ConditionsTN 17 08-18
DI 23022.085Acute LeukemiaTN 1 10-08
DI 23022.090Adrenal CancerTN 1 10-08
DI 23022.095Alexander DiseaseTN 16 03-18
DI 23022.100Amyotrophic Lateral Sclerosis (ALS)TN 1 10-08
DI 23022.105Anaplastic Adrenal Cancer - AdultTN 1 10-08
DI 23022.106AngiosarcomaTN 10 01-14
DI 23022.110Astrocytoma - Grade III and IVTN 1 10-08
DI 23022.111Atypical Teratoid/Rhabdoid TumorTN 10 01-14
DI 23022.115Bladder CancerTN 1 10-08
DI 23022.120OsteosarcomaTN 7 08-12
DI 23022.125Breast CancerTN 1 10-08
DI 23022.127CACH- Vanishing White Matter Disease- Congenital, Infantile and Early Childhood Onset FormsTN 15 09-17
DI 23022.130Canavan DiseaseTN 16 03-18
DI 23022.135Cerebro Oculo Facio Skeletal (COFS) SyndromeTN 1 10-08
DI 23022.136Chronic Idiopathic Intestinal Pseudo ObstructionTN 10 01-14
DI 23022.140Chronic Myelogenous Leukemia (CML) - Blast PhaseTN 1 10-08
DI 23022.141Coffin-Lowry SyndromeTN 16 03-18
DI 23022.143Congenital Myotonic DystrophyTN 15 09-17
DI 23022.145Creutzfeldt-Jakob Disease (CJD)TN 16 03-18
DI 23022.150Ependymoblastoma (Child Brain Cancer)TN 13 09-15
DI 23022.155Esophageal CancerTN 1 10-08
DI 23022.156EsthesioneuroblastomaTN 10 01-14
DI 23022.160Farber's DiseaseTN 16 03-18
DI 23022.163Fibrolamellar CancerTN 17 08-18
DI 23022.165Friedreich's Ataxia (FRDA)TN 16 03-18
DI 23022.170Frontotemporal Dementia (FTD), Pick's Disease -Type ATN 16 03-18
DI 23022.175Gallbladder CancerTN 1 10-08
DI 23022.180Gaucher Disease (GD) - Type 2TN 1 10-08
DI 23022.181Giant Axonal NeuropathyTN 16 03-18
DI 23022.185Glioblastoma Multiforme (Brain Cancer)TN 1 10-08
DI 23022.190Head and Neck CancersTN 16 03-18
DI 23022.191Hoyeraal-Hreidarsson SyndromeTN 16 03-18
DI 23022.195Infantile Neuroaxonal Dystrophy (INAD)TN 16 03-18
DI 23022.200Inflammatory Breast CancerTN 1 10-08
DI 23022.201Intracranial HemangiopericytomaTN 10 01-14
DI 23022.202Joubert SyndromeTN 16 03-18
DI 23022.205Kidney CancerTN 1 10-08
DI 23022.207Kleefstra SyndromeTN 15 09-17
DI 23022.210Krabbe Disease (KD) - InfantileTN 16 03-18
DI 23022.215Large Intestine CancerTN 1 10-08
DI 23022.216Leptomeningeal CarcinomatosisTN 10 01-14
DI 23022.220Lesch-Nyhan Syndrome (LNS)TN 16 03-18
DI 23022.221Liposarcoma - Metastatic or RecurrentTN 10 01-14
DI 23022.225Liver CancerTN 1 10-08
DI 23022.226Malignant EctomesenchymomaTN 10 01-14
DI 23022.227Malignant Renal Rhabdoid TumorTN 10 01-14
DI 23022.230Mantle Cell Lymphoma (MCL)TN 1 10-08
DI 23022.231Marshall-Smith SyndromeTN 10 01-14
DI 23022.233Megacystis Microcolon Intestinal Hypoperistalsis SyndromeTN 17 08-18
DI 23022.234Megalencephaly-Capillary Malformation SyndromeTN 17 08-18
DI 23022.235Metachromatic Leukodystrophy (MLD)TN 16 03-18
DI 23022.240Niemann-pick Disease (NPD) - Type ATN 1 10-08
DI 23022.245Non-Small Cell Lung CancerTN 1 10-08
DI 23022.246Oligodendroglioma Brain Cancer - Grade IIITN 13 09-15
DI 23022.250Ornithine Transcarbamylase (OTC) DeficiencyTN 16 03-18
DI 23022.255Osteogenesis Imperfecta (OI) - Type IITN 1 10-08
DI 23022.260Ovarian CancerTN 1 10-08
DI 23022.261Pallister-Killian SyndromeTN 16 03-18
DI 23022.265Pancreatic CancerTN 1 10-08
DI 23022.270Peritoneal MesotheliomaTN 1 10-08
DI 23022.275Pleural MesotheliomaTN 1 10-08
DI 23022.280Pompe Disease - InfantileTN 16 03-18
DI 23022.281Progressive Bulbar PalsyTN 16 03-18
DI 23022.282Prostate Cancer - Hormone Refractory Disease – or with Visceral MetastasesTN 10 01-14
DI 23022.285Rett (RTT) SyndromeTN 16 03-18
DI 23022.286Revesz SyndromeTN 10 01-14
DI 23022.290Salivary CancersTN 1 10-08
DI 23022.295Sandhoff DiseaseTN 1 10-08
DI 23022.296Seckel SyndromeTN 16 03-18
DI 23022.297Sjogren-Larsson SyndromeTN 16 03-18
DI 23022.300Small Cell Cancer of the Large IntestineTN 16 03-18
DI 23022.305Small Cell Cancer of the OvaryTN 1 10-08
DI 23022.310Small Cell Cancer of the ProstateTN 1 10-08
DI 23022.311Small Cell Cancer of the ThymusTN 10 01-14
DI 23022.315Small-Cell Cancer of the Female Genital TractTN 13 09-15
DI 23022.320Small Cell Lung CancerTN 1 10-08
DI 23022.325Small Intestine CancerTN 1 10-08
DI 23022.326Soft Tissue Sarcoma - with Distant Metastases or RecurrentTN 10 01-14
DI 23022.330Spinal Muscular Atrophy (SMA) - Types 0 and 1TN 16 03-18
DI 23022.335Stomach CancerTN 1 10-08
DI 23022.337Superficial Siderosis of the Central Nervous SystemTN 17 08-18
DI 23022.340Thyroid CancerTN 1 10-08
DI 23022.343Tetrasomy 18pTN 17 08-18
DI 23022.345Ureter CancerTN 1 10-08
DI 23022.346X-Linked Lymphoproliferative DiseaseTN 10 01-14
DI 23022.347X-Linked Myotubular MyopathyTN 16 03-18
DI 23022.350Alstrom SyndromeTN 3 02-10
DI 23022.355Amegakaryocytic ThrombocytopeniaTN 3 02-10
DI 23022.360Ataxia TelangiectasiaTN 16 03-18
DI 23022.365Batten DiseaseTN 16 03-18
DI 23022.370Bilateral RetinoblastomaTN 3 02-10
DI 23022.375Cri du Chat SyndromeTN 3 02-10
DI 23022.380Degos Disease, SystemicTN 3 02-10
DI 23022.385Early-Onset Alzheimer's DiseaseTN 16 03-18
DI 23022.390Edwards Syndrome (Trisomy 18)TN 3 02-10
DI 23022.395Fibrodysplasia Ossificans ProgressivaTN 3 02-10
DI 23022.400Fukuyama Congenital Muscular DystrophyTN 16 03-18
DI 23022.405Hemophagocytic LymphohistiocytosisTN 3 02-10
DI 23022.410Hunter SyndromeTN 3 02-10
DI 23022.415Hurler SyndromeTN 3 02-10
DI 23022.420Idiopathic Pulmonary FibrosisTN 3 02-10
DI 23022.425Infantile Neuronal Ceroid-LipofuscinosesTN 16 03-18
DI 23022.430Junctional Epidermolysis Bullosa Lethal TypeTN 3 02-10
DI 23022.435Late Infantile Neuronal Ceroid-LipofuscinosesTN 16 03-18
DI 23022.440Leigh's DiseaseTN 3 02-10
DI 23022.445Maple Syrup Urine DiseaseTN 16 03-18
DI 23022.450Merosin Deficient Congenital Muscular DystrophyTN 16 03-18
DI 23022.455Mixed DementiaTN 16 03-18
DI 23022.460Mucosal MelanomaTN 3 02-10
DI 23022.465Neonatal AdrenoleukodystrophyTN 3 02-10
DI 23022.470(Neonatal) Glutaric AcidemiaTN 3 02-10
DI 23022.475Niemann-Pick Type CTN 3 02-10
DI 23022.480Patau Syndrome (Trisomy 13)TN 3 02-10
DI 23022.485Primary Progressive AphasiaTN 3 02-10
DI 23022.490Progressive Multifocal LeukoencephalopathyTN 16 03-18
DI 23022.495Sanfilippo SyndromeTN 3 02-10
DI 23022.500Spinocerebellar AtaxiaTN 3 02-10
DI 23022.505Subacute Sclerosing PanencephalitisTN 16 03-18
DI 23022.510Tay Sachs Disease, Infantile TypeTN 3 02-10
DI 23022.515Thanatophoric Dysplasia, Type 1TN 3 02-10
DI 23022.520Ullrich Congenital Muscular DystrophyTN 16 03-18
DI 23022.525Walker Warburg SyndromeTN 16 03-18
DI 23022.530Wolman DiseaseTN 3 02-10
DI 23022.535Zellweger SyndromeTN 3 02-10
DI 23022.540Aortic AtresiaTN 5 07-11
DI 23022.545Eisenmenger SyndromeTN 5 07-11
DI 23022.550Endomyocardial FibrosisTN 5 07-11
DI 23022.555Heart Transplant Graft FailureTN 5 07-11
DI 23022.560Heart Transplant Wait List 1A/1BTN 5 07-11
DI 23022.565Hypoplastic Left Heart SyndromeTN 5 07-11
DI 23022.570Ventricular Assist Device Recipient — Left, Right, or BiventricularTN 11 04-14
DI 23022.575Mitral Valve AtresiaTN 5 07-11
DI 23022.580Cardiac Amyloidosis- AL TypeTN 12 09-15
DI 23022.585Pulmonary AtresiaTN 5 07-11
DI 23022.590Single VentricleTN 5 07-11
DI 23022.595Tricuspid AtresiaTN 5 07-11
DI 23022.600Angelman SyndromeTN 16 03-18
DI 23022.605Corticobasal DegenerationTN 16 03-18
DI 23022.610Lewy Body DementiaTN 16 03-18
DI 23022.615Lowe SyndromeTN 6 12-11
DI 23022.620Malignant Multiple SclerosisTN 16 03-18
DI 23022.625Multicentric Castleman DiseaseTN 16 03-18
DI 23022.630Multiple System AtrophyTN 16 03-18
DI 23022.635Paraneoplastic PemphigusTN 6 12-11
DI 23022.640Primary Central Nervous System LymphomaTN 16 03-18
DI 23022.645Primary Effusion LymphomaTN 16 03-18
DI 23022.650Progressive Supranuclear PalsyTN 16 03-18
DI 23022.655Pulmonary Kaposi SarcomaTN 16 03-18
DI 23022.660The ALS Parkinsonism Dementia ComplexTN 16 03-18
DI 23022.665Aicardi--Goutieres SyndromeTN 16 03-18
DI 23022.670Alobar HoloprosencephalyTN 7 08-12
DI 23022.675Alpers DiseaseTN 16 03-18
DI 23022.680Alpha Mannosidosis--Type II and IIITN 16 03-18
DI 23022.685Carcinoma of Unknown Primary SiteTN 7 08-12
DI 23022.690Cerebrotendinous XanthomatosisTN 16 03-18
DI 23022.695Child Neuroblastoma—with distant metastases or recurrentTN 7 08-12
DI 23022.700Child LymphomaTN 13 09-15
DI 23022.705Chondrosarcoma—with multimodal therapyTN 7 08-12
DI 23022.710Cornelia de Lange Syndrome--Classic FormTN 7 08-12
DI 23022.715Ewing SarcomaTN 7 08-12
DI 23022.720Follicular Dendritic Cell Sarcoma-- metastatic or recurrentTN 7 08-12
DI 23022.725Fucosidosis--Type ITN 7 08-12
DI 23022.730Galactosialidosis--Early and Late Infantile TypesTN 7 08-12
DI 23022.735Glioma - Grade III and IVTN 7 08-12
DI 23022.745HepatoblastomaTN 7 08-12
DI 23022.750Histiocytosis SyndromesTN 7 08-12
DI 23022.755Hutchinson-Gilford Progeria SyndromeTN 7 08-12
DI 23022.760HydranencephalyTN 7 08-12
DI 23022.765Hypocomplementemic Urticarial Vasculitis SyndromeTN 7 08-12
DI 23022.770Hypophosphatasia--Perinatal (Lethal) and Infantile Onset TypesTN 7 08-12
DI 23022.775I Cell DiseaseTN 7 08-12
DI 23022.780Infantile Free Sialic Acid Storage DiseaseTN 7 08-12
DI 23022.785Juvenile Onset Huntington DiseaseTN 16 03-18
DI 23022.790Kufs Disease--Type A and BTN 16 03-18
DI 23022.795LissencephalyTN 16 03-18
DI 23022.800Lymphomatoid Granulomatosis--Grade IIITN 7 08-12
DI 23022.805Malignant Brain Stem Gliomas--ChildhoodTN 7 08-12
DI 23022.810Skin Malignant Melanoma with MetastasesTN 14 07-16
DI 23022.815Mastocytosis--Type IVTN 7 08-12
DI 23022.820MedulloblastomaTN 13 09-15
DI 23022.825Merkel Cell Carcinoma – with metastasesTN 7 08-12
DI 23022.830Myoclonic Epilepsy with Ragged Red Fibers SyndromeTN 16 03-18
DI 23022.835Nephrogenic Systemic FibrosisTN 7 08-12
DI 23022.836Neurodegeneration with Brain Iron Accumulation- Type 1 and 2TN 16 03-18
DI 23022.840Obliterative BronchiolitisTN 7 08-12
DI 23022.845Ohtahara SyndromeTN 16 03-18
DI 23022.850Orthochromatic Leukodystrophy with Pigmented GliaTN 16 03-18
DI 23022.855Pearson SyndromeTN 7 08-12
DI 23022.860Pelizaeus-Merzbacher Disease--Classic FormTN 16 03-18
DI 23022.865Pelizaeus-Merzbacher Disease--Connatal FormTN 16 03-18
DI 23022.870Peripheral Nerve Cancer – metastatic or recurrentTN 7 08-12
DI 23022.875Perry SyndromeTN 16 03-18
DI 23022.880RhabdomyosarcomaTN 7 08-12
DI 23022.885Rhizomelic Chondrodysplasia PunctataTN 7 08-12
DI 23022.890Schindler Disease--Type ITN 7 08-12
DI 23022.895Smith Lemli Opitz SyndromeTN 7 08-12
DI 23022.900Spinal Nerve Root Cancer – metastatic or recurrentTN 7 08-12
DI 23022.905Stiff Person SyndromeTN 16 03-18
DI 23022.910Tabes DorsalisTN 16 03-18
DI 23022.915Wolf-Hirschhorn SyndromeTN 7 08-12
DI 23022.920Xeroderma PigmentosumTN 7 08-12
DI 23022.921Adult Non-Hodgkin LymphomaTN 8 11-12
DI 23022.923Adult Onset Huntington DiseaseTN 16 03-18
DI 23022.925Allan-Herndon-Dudley SyndromeTN 16 03-18
DI 23022.927Alveolar Soft Part SarcomaTN 8 11-12
DI 23022.929Aplastic AnemiaTN 8 11-12
DI 23022.931Beta Thalassemia MajorTN 8 11-12
DI 23022.933Bilateral Optic Atrophy- InfantileTN 8 11-12
DI 23022.935Caudal Regression Syndrome- Types III and IVTN 16 03-18
DI 23022.937Child Lymphoblastic LymphomaTN 13 09-15
DI 23022.939Congenital LymphedemaTN 8 11-12
DI 23022.941De Sanctis Cacchione SyndromeTN 16 03-18
DI 23022.943Dravet SyndromeTN 8 11-12
DI 23022.945Endometrial Stromal SarcomaTN 8 11-12
DI 23022.947Erdheim Chester DiseaseTN 8 11-12
DI 23022.949Fatal Familial InsomniaTN 16 03-18
DI 23022.951Fryns SyndromeTN 8 11-12
DI 23022.953Fulminant Giant Cell MyocarditisTN 8 11-12
DI 23022.955Hepatopulmonary SyndromeTN 8 11-12
DI 23022.957Hepatorenal SyndromeTN 8 11-12
DI 23022.959Jervell and Lange-Nielsen SyndromeTN 8 11-12
DI 23022.961LeiomyosarcomaTN 8 11-12
DI 23022.963Malignant Gastrointestinal Stromal TumorTN 8 11-12
DI 23022.965Malignant Germ Cell TumorTN 8 11-12
DI 23022.967MECP2 Duplication SyndromeTN 16 03-18
DI 23022.969Menkes Disease- Classic or Infantile Onset FormTN 8 11-12
DI 23022.971NFU-1 Mitochondrial DiseaseTN 8 11-12
DI 23022.973Nonketotic HyperglycinemiaTN 16 03-18
DI 23022.975Peritoneal Mucinous CarcinomatosisTN 8 11-12
DI 23022.977Phelan-Mcdermid SyndromeTN 16 03-18
DI 23022.979Retinopathy of Prematurity- Stage VTN 8 11-12
DI 23022.981Roberts SyndromeTN 16 03-18
DI 23022.983Severe Combined Immunodeficiency -- ChildhoodTN 8 11-12
DI 23022.985Sinonasal CancerTN 8 11-12
DI 23022.987Transplant Coronary Artery VasculopathyTN 8 11-12
DI 23022.989Usher Syndrome- Type ITN 8 11-12

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DI 23022.000 - Processing Quick Disability Determination (QDD) and Compassionate Allowance (CAL) in the Disability Determination Services (DDS) - Table of Contents - 03/28/2018
Batch run: 08/17/2018
Rev:03/28/2018