DI 23022.080:
List of Compassionate Allowance (CAL) Conditions
Effective Dates: 09/15/2017 - Present
- Effective Dates: 08/17/2018 - Present
TN 15 (09-17)
- TN 17 (08-18)
- DI 23022.080 List of Compassionate Allowance (CAL) Conditions
- The following is a complete list of CAL conditions:
- Section Title
- Section Number
- Acute Leukemia
- DI 23022.085
- Adrenal Cancer -- with distant metastases or inoperable, unresectable or recurrent
- DI 23022.090
- Adult Non-Hodgkin Lymphoma
- DI 23022.921
- Adult Onset Huntington Disease
- DI 23022.923
- Aicardi-Goutieres Syndrome
- DI 23022.665
- Alexander Disease (ALX) -- Neonatal and Infantile
- DI 23022.095
- Allan-Herndon-Dudley Syndrome
- DI 23022.925
- Alobar Holoprosencephaly
- DI 23022.670
- Alpers Disease
- DI 23022.675
Alpha Mannosidosis - Type II and III
- Alpha Mannosidosis -- Type II and III
- DI 23022.680
- Alstrom Syndrome
- DI 23022.350
- Alveolar Soft Part Sarcoma
- DI 23022.927
- Amegakaryocytic Thrombocytopenia
- DI 23022.355
- Amyotrophic Lateral Sclerosis (ALS)
- DI 23022.100
- Anaplastic Adrenal Cancer -- with distant metastases or inoperable, unresectable or recurrent
- DI 23022.105
- Angelman Syndrome
- DI 23022.600
- Aortic Atresia
- DI 23022.540
- Angiosarcoma
- DI 23022.106
- Aplastic Anemia
- DI 23022.929
- Astrocytoma -- GRADE III and IV
- DI 23022.110
- Ataxia Telangiectasia
- DI 23022.360
- Atypical Teratoid/Rhabdoid Tumor
- DI 23022.111
- Batten Disease
- DI 23022.365
- Beta Thalassemia Major
- DI 23022.931
Bilateral Optic Atrophy- Infantile
- Bilateral Optic Atrophy -- Infantile
- DI 23022.933
- Bilateral Retinoblastoma
- DI 23022.370
- Bladder Cancer -- with distant metastases or inoperable or unresectable
- DI 23022.115
- Breast Cancer -- with distant metastases or inoperable or unresectable
- DI 23022.125
CACH- Vanishing White Matter Disease- Infantile and Childhood Onset Forms
- CACH -- Vanishing White Matter Disease -- Infantile and Childhood Onset Forms
- DI 23022.127
- Canavan Disease (CD)
- DI 23022.130
- Carcinoma of Unknown Primary Site
- DI 23022.685
- Cardiac Amyloidosis- AL Type
- DI 23022.580
- Caudal Regression Syndrome- Types III and IV
- DI 23022.935
- Cerebro Oculo Facio Skeletal (COFS) Syndrome
- DI 23022.135
- Cerebrotendinous Xanthomatosis
- DI 23022.690
- Child Neuroblastoma- - with distant metastasis or recurrent
- DI 23022.695
- Child Non-Hodgkin Lymphoma- - recurrent
- DI 23022.700
- Child T-Cell Lymphoblastic Lymphoma
- DI 23022.937
- Chondrosarcoma- - with multimodal therapy
- DI 23022.705
- Chronic Idiopathic Intestinal Pseudo Obstruction
- DI 23022.136
- Chronic Myelogenous Leukemia -- Blast Phase
- DI 23022.140
- Coffin-Lowry Syndrome
- DI 23022.141
- Congenital Lymphedema
- DI 23022.939
- Congenital Myotonic Dystrophy
- DI 23022.143
- Cornelia de Lange Syndrome- - Classic Form
- DI 23022.710
- Corticobasal Degeneration
- DI 23022.605
- Creutzfeldt-Jakob Disease (CJD) -- Adult
- DI 23022.145
- Cri du Chat Syndrome
- DI 23022.375
- Degos Disease, Systemic
- DI 23022.380
- DeSanctis Cacchione Syndrome
- DI 23022.941
- Dravet Syndrome
- DI 23022.943
- Early-Onset Alzheimer’s Disease
- DI 23022.385
- Edwards Syndrome (Trisomy 18)
- DI 23022.390
- Eisenmenger Syndrome
- DI 23022.545
- Endometrial Stromal Sarcoma
- DI 23022.945
- Endomyocardial Fibrosis
- DI 23022.550
- Ependymoblastoma (Child Brain Tumor)
- DI 23022.150
- Esophageal Cancer
- DI 23022.155
- Esthesioneuroblastoma
- DI 23022.156
- Ewing Sarcoma
- DI 23022.715
- Farber’s Disease (FD) -- Infantile
- DI 23022.160
- Fatal Familial Insomnia
- DI 23022.949
- Fibrodysplasia Ossificans Progressiva
- DI 23022.395
Follicular Dendritic Cell Sarcoma - - metastatic or recurrent
- Fibrolamellar Cancer
- DI 23022.163
- Follicular Dendritic Cell Sarcoma -- metastatic or recurrent
- DI 23022.720
- Friedreichs Ataxia (FRDA)
- DI 23022.165
Frontotemporal Dementia (FTD) Picks Disease --Type A – Adult
- Frontotemporal Dementia (FTD) Picks Disease -- Type A – Adult
- DI 23022.170
- Fryns Syndrome
- DI 23022.951
- Fucosidosis – Type I
- DI 23022.725
- Fukuyama Congenital Muscular Dystrophy
- DI 23022.400
- Fulminant Giant Cell Myocarditis
- DI 23022.953
- Galactosialidosis – Early and Late Infantile Types
- DI 23022.730
- Gallbladder Cancer
- DI 23022.175
- Gaucher Disease (GD) --Type 2
- DI 23022.180
- Glioblastoma Multiforme (Brain Tumor)
- DI 23022.185
- Glioma Grade III and IV
- DI 23022.735
- Giant Axonal Neuropathy
- DI 23022.181
- Gluteric Acidemia – Type II
- DI 23022.470
- Head and Neck Cancers -- with distant metastasis or inoperable or uresectable
- DI 23022.190
- Heart Transplant Graft Failure
- DI 23022.555
- Heart Transplant Wait List – 1A/1B
- DI 23022.560
- Hemophagocytic Lymphohistiocytosis
- DI 23022.405
- Hepatoblastoma
- DI 23022.745
- Hepatopulmonary Syndrome
- DI 23022.955
- Hepatorenal Syndrome
- DI 23022.957
- Histiocytosis Syndromes
- DI 23022.750
- Hoyeaal-Hreidarsson Syndrome
- DI 23022.191
- Hutchinson-Gilford Progeria Syndrome
- DI 23022.755
- Hydranencephaly
- DI 23022.760
- Hypocomplementemic Urticarial Vasculitis Syndrome
- DI 23022.765
- Hypophosphatasia- Perinatal (Lethal) and Infantile Onset Types
- DI 23022.770
- Hypoplastic Left Heart Syndrome
- DI 23022.565
- I Cell Disease
- DI 23022.775
- Idiopathic Pulmonary Fibrosis
- DI 23022.420
- Infantile Free Sialic Acid Storage Disease
- DI 23022.780
- Infantile Neuroaxonal Dystrophy (INAD)
- DI 23022.195
- Infantile Neuronal Ceroid-Lipofuscinoses
- DI 23022.425
- Inflammatory Breast Cancer (IBC)
- DI 23022.200
- Intracranial Hemangiopericytoma
- DI 23022.201
- Jervell and Lange-Nielsen Syndrome
- DI 23022.959
- Joubert Syndrome
- DI 23022.202
- Junctional Epidermolysis Bullosa Lethal Type
- DI 23022.430
- Juvenile Onset Huntington Disease
- DI 23022.785
- Kidney Cancer -- inoperable or unresectable
- DI 23022.205
- Kleefstra Syndrome
- DI 23022.207
- Krabbe Disease (KD) --Infantile
- DI 23022.210
- Kufs Disease Type A and B
- DI 23022.790
- Large Intestine Cancer -- with distant metastasis or inoperable, unresectable or recurrent
- DI 23022.215
- Late Infantile Neuronal Ceroid-Lipofuscinoses
- DI 23022.435
- Leigh’s Disease
- DI 23022.440
- Leiomyosarcoma
- DI 23022.961
- Leptomeningeal Carcinomatosis
- DI 23022.216
- Lesch-Nyhan Syndrome (LNS)
- DI 23022.220
- Lewy Body Dementia
- DI 23022.610
- Liposarcoma – metastatic or recurrent
- DI 23022.221
- Lissencephaly
- DI 23022.795
- Liver Cancer
- DI 23022.225
- Lowe Syndrome
- DI 23022.615
- Lymphomatoid Granulomatosis - Grade III
- DI 23022.800
- Malignant Brain Stem Gliomas - Childhood
- DI 23022.805
- Malignant Ectomesenchymoma
- DI 23022.226
- Malignant Gastrointestinal Stromal Tumor
- DI 23022.963
- Malignant Germ Cell Tumor
- DI 23022.965
- Malignant Multiple Sclerosis
- DI 23022.620
- Malignant Renal Rhabdoid Tumor
- DI 23022.227
- Mantle Cell Lymphoma (MCL)
- DI 23022.230
- Maple Syrup Urine Disease
- DI 23022.445
- Marshall-Smith Syndrome
- DI 23022.231
- Mastocytosis - Type IV
- DI 23022.815
- MECP 2 Duplication Syndrome
- DI 23022.967
- Medulloblastoma - with metastasis
- DI 23022.820
- Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
- DI 23022.233
- Megalencephaly-Capillary Malformation Syndrome
- DI 23022.234
- Menkes Disease - Classic or Infantile Onset Form
- DI 23022.969
- Merkel Cell Carcinoma - with metastasis
- DI 23022.825
- Merosin Deficient Congenital Muscular Dystrophy
- DI 23022.450
- Metachromatic Leukodystrophy - Late Infantile
- DI 23022.235
- Mitral Valve Atresia
- DI 23022.575
- Mixed Dementia
- DI 23022.455
- MPS I, formerly known as Hurler Syndrome
- DI 23022.415
- MPS II, formerly known as Hunter Syndrome
- DI 23022.410
- MPS III, formerly known as Sanfilippo Syndrome
- DI 23022.495
- Mucosal Melanoma
- DI 23022.460
- Multicentric Castleman Disease
- DI 23022.625
- Multiple System Atrophy
- DI 23022.630
- Myocolonic Epilepsy and Ragged Red Fibers Syndrome
- DI 23022.830
- Neonatal Adrenoleukodystrophy
- DI 23022.465
- (Neonatal) Glutaric Acidemia
- DI 23022.470
- Nephrogenic Systemic Fibrosis
- DI 23022.835
- NFU-1 Mitochondrial Disease
- DI 23022.971
- Niemann-Pick Disease (NPD) -- type A
- DI 23022.240
- Niemann-Pick Disease Type C
- DI 23022.475
- Nonketotic Hyperglycinemia
- DI 23022.973
- Non-Small Cell Lung Cancer -- with metastases to or beyond the hilar nodes or inoperable, unresectable or recurrent
- DI 23022.245
- Obliterative Bronchiolitis
- DI 23022.840
- Ohtahara Syndrome
- DI 23022.845
- Oligodendroglioma Brain Tumor- Grade III
- DI 23022.246
- Ornithine Transcarbamylase (OTC) Deficiency
- DI 23022.250
- Orthochromatic Leukodystrophy with Pigmented Glia
- DI 23022.850
- Osteogenesis Imperfecta (OI) -- Type II
- DI 23022.255
- Osteosarcoma, formerly known as Bone Cancer -- with distant metastases or inoperable or unresectable
- DI 23022.120
- Ovarian Cancer -- with distant metastases or inoperable or unresectable
- DI 23022.260
- Pallister-Killian Syndrome
- DI 23022.261
- Pancreatic Cancer
- DI 23022.265
- Paraneoplastic Pemphigus
- DI 23022.635
- Patau Syndrome (Trisomy 13)
- DI 23022.480
- Pearson Syndrome
- DI 23022.855
- Pelizaeus-Merzbacher Disease- - Classic Form
- DI 23022.860
- Pelizaeus-Merzbacher Disease- - Connatal Form
- DI 23022.865
- Peripheral Nerve Cancer- - metastatic or recurrent
- DI 23022.870
- Peritoneal Mesothelioma
- DI 23022.270
- Peritoneal Mucinous Carcinomatosis
- DI 23022.975
- Perry Syndrome
- DI 23022.875
- Phelan-McDermid Syndrome
- DI 23022.977
- Pleural Mesothelioma
- DI 23022.275
- Pompe Disease -- Infantile
- DI 23022.280
- Primary Central Nervous System Lymphoma
- DI 23022.640
- Primary Effusion Lymphoma
- DI 23022.645
- Primary Progressive Aphasia
- DI 23022.485
- Progressive Bulbar Palsy
- DI 23022.281
- Progressive Multifocal Leukoencephalopathy
- DI 23022.490
- Progressive Supranuclear Palsy
- DI 23022.650
- Prostate Cancer- Hormone Refractory Disease— or with visceral metastases
- DI 23022.282
- Pulmonary Atresia
- DI 23022.585
- Pulmonary Kaposi Sarcoma
- DI 23022.655
- Retinopathy of Prematurity- Stage V
- DI 23022.979
- Rett (RTT) Syndrome
- DI 23022.285
- Revesez Syndrome
- DI 23022.286
- Rhabdomyosarcoma
- DI 23022.880
- Rhizomelic Chondrodysplasia Punctata
- DI 23022.885
- Roberts Syndrome
- DI 23022.981
- Salivary Tumors
- DI 23022.290
- Sandhoff Disease
- DI 23022.295
- Schindler Disease - - Type I
- DI 23022.890
- Seckel Syndrome
- DI 23022.296
- Severe Combined Immunodeficiency- Childhood
- DI 23022.983
- Single Ventricle
- DI 23022.590
- Sinonasal Cancer
- DI 23022.985
- Sjogren-Larsson Syndrome
- DI 23022.297
- Skin Malignant Melanoma—with metastases
- DI 23022.810
Small -Cell Cancer of the Large Intestine
- Small-Cell Cancer of the Large Intestine
- DI 23022.300
Small- Cell Cancer of the Ovary
- Small-Cell Cancer of the Ovary
- DI 23022.305
Small- Cell Cancer of the Prostate
- Small-Cell Cancer of the Prostate
- DI 23022.310
Small- Cell Cancer of the Thymus
- Small-Cell Cancer of the Thymus
- DI 23022.311
Small- Cell Cancer of the Uterus
- Small-Cell Cancer of the Uterus
- DI 23022.315
Small- Cell Lung Cancer
- Small-Cell Lung Cancer
- DI 23022.320
- Small Intestine Cancer -- with distant metastases or inoperable, unresectable or recurrent
- DI 23022.325
- Smith Lemli Opitz Syndrome
- DI 23022.895
- Soft Tissue Sarcoma – with distant metastases or recurrent
- DI 23022.326
- Spinal Muscular Atrophy (SMA) -- Types 0 and 1
- DI 23022.330
- Spinal Nerve Root Cancer- - metastatic or recurrent
- DI 23022.900
- Spinocerebellar Ataxia
- DI 23022.500
- Stiff Person Syndrome
- DI 23022.905
- Stomach Cancer -- with distant metastases or inoperable, unresectable or recurrent
- DI 23022.335
- Subacute Sclerosing Panencephalitis
- DI 23022.505
- Superficial Siderosis of the Central Nervous System
- DI 23022.337
- Tabes Dorsalis
- DI 23022.910
- Tay Sachs Disease
- DI 23022.510
- Tetrasomy 18p
- DI 23022.343
- Thanatophoric Dysplasia, Type 1
- DI 23022.515
- The ALS/Parkinsonism Dementia Complex
- DI 23022.660
- Thyroid Cancer
- DI 23022.340
- Transplant Coronary Artery Vasculopathy
- DI 23022.987
- Tricuspid Atresia
- DI 23022.595
- Ullrich Congenital Muscular Dystrophy
- DI 23022.520
- Ureter Cancer -- with distant metastases or inoperable, unresectable or recurrent
- DI 23022.345
- Usher Syndrome- Type I
- DI 23022.989
- Ventricular Assist Device Recipient
- DI 23022.570
- Walker Warburg Syndrome
- DI 23022.525
- Wolf-Hirschhorn Syndrome
- DI 23022.915
- Wolman Disease
- DI 23022.530
- Xeroderma Pigmentosum
- DI 23022.920
- X-Linked Lymphoproliferative Disease
- DI 23022.346
- X-Linked Myotubular Myopathy
- DI 23022.347
- Zellweger Syndrome
- DI 23022.535
x
← This means that the line
was removed and
was added – in other words, the "Effective Dates" line at the top of the document has been updated to reflect that the new version is effective as of the date the change was made.