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DISEASE ENTITY
Viral Conditions (5)
- HIV 1 (no AIDS diagnosis)*
- AIDS (advanced)*
- Hepatitis C*
- Epstein Barr*
- Lyme Disease*
Ocular Conditions (4)
- Retinitis Pigmentosa*
- Macular Degeneration*
- Glaucoma*
- Optic Atrophy
Endocrine diseases (4)
- Diabetes
- Adrenal Disease
- Addison’s Disease*
- Cushings Syndrome
Accelerated Surgery or Accident Recovery* (2)
Cardiology(4)
- Myocardial Infarction
- Dilated Cardiomyopathy*
- Atherosclerosis
- Congestive Heart Failure
Autoimmune (5)
- Multiple sclerosis
- Crohn’s Disease*
- Rheumatoid Arthritis*
- Lupus
- Scleroderma*
Renal Disease (2)
- Acute renal failure
- Glomerulonephritis
Lung Disease (4)
- Progressive Dyspnea*
- COPD
- Bronchial Asthma
- Scleroderma
Neurological Disease (16)
- Duchanne’s Muscular Dystrophy*
- Polymyositis*
- Multiple Sclerosis (MS)*
- Amyotrophic Lateral Sclerosis (ALS)*
- Parkinson’s Disease (PD)*
- Cerebral Palsy (CP)*
- Guilliame Barre*
- Transverse Myelitis*
- Basal Ganglia*
- Supranuclear Palsy*
- Huntington’s Disease*
- Rhett’s Syndrome*
- Neurological Injury
- Acute and Chronic Stroke*
- Spinal Cord Injury*
- Nerve Injury*
- Traumatic Brain Injury*
Gastroenterology (3)
- Crohns disease
- Liver Disease
- Hepatitis B*
- Hepatitis C*
Cancer (46)
- Acute Leukemias
- Acute Lymphoblastic Leukemia (ALL)
- Acute Myelogenous Leukemia (AML)
- Acute Biphenotypic Leukemia
- Acute Undifferentiated Leukemia
- Chronic Leukemias
- Chronic Myelogenous Leukemia (CML)
- Chronic Lymphocytic Leukemia (CLL)
- Juvenile Chronic Myelogenous Leukemia (JCML)
- Juvenile Myelomonocytic Leukemia (JMML)
- Myelodysplastic Syndromes
- Myelodysplastic Syndrome
- Refractory Anemia (RA)
- Refractory Anemia with Ringed Sideroblasts (RARS)
- Refractory Anemia with Excess Blasts (RAEB)
- Refractory Anemia with Excess Blasts in Transformation (RAEB-T)
- Chronic Myelomonocytic Leukemia (CMML)
- Hematopoietic Cell Disorders
- Aplastic Anemia (Severe)
- Fanconi Anemia
- Paroxysmal Nocturnal Hemoglobinuria (PNH)
- Pure Red Cell Aplasia
- Myeloproliferative Disorders
- Acute Myelofibrosis
- Agnogenic Myeloid Metaplasia (myelofibrosis)
- Polycythemia Vera
- Essential Thrombocythemia
- Plasma Cell Disorders
- Multiple Myeloma
- Plasma Cell Leukemia
- Waldenstrom's Macroglobulinemia
- Lymphoproliferative Disorders
- Non-Hodgkin's Lymphoma
- Hodgkin's Disease
- Phagocyte Disorders
- Acute Lympholastic Leukemia*
- Non-Hodgkin’s Lymphoma*
- Acute lymphocytic leukemia
- Acute myelocytic leukemia
- Juvenile chronic myelogenous leukemia
- Neuroblastoma
- Chronic myelogenous leukemia
- Organ/Tissue Cancers (Immunotherapy)
- Breast Cancer*
- Prostate Cancer*
- Colon Cancer*
- Pancreatic Cancer*
- Lung Cancer*
- Malignant Melanoma*
- Chemo Rescue*
- Ewing Sarcoma
- Neuroblastoma
- Renal Cell Carcinoma
Hematology (22)
- Chediak-Higashi Syndrome
- Chronic Granulomatous Disease
- Neutrophil Actin Deficiency
- Reticular Dysgenesis
- Anemia
- Fanconi anemia
- Aplastic anemia
- Refractory anemia
- Thalassemia
- Sickle cell anemia
- Amegakaryocytic thrombocytopenia
- Kostmann syndrome
- Blackfan-Diamond syndrome
- Severe combined immunodeficiency
- X-linked lymphoproliferative disorder
- Wiskott-Aldrich syndrome
- Hurler syndrome
- Hunter syndrome
- Gunther disease
- Osteopetrosis
- Globoid cell leukodystrophy
- Adrenoleukodystrophy
- Wiscott-Aldrich’s Syndrome*
Inherited Metabolic Disorders (15)
- Mucopolysaccharidoses (MPS)
- Hurler's Syndrome (MPS-IH)
- Scheie Syndrome (MPS-IS)
- Hunter's Syndrome (MPS-II)
- Sanfilippo Syndrome (MPS-III)
- Morquio Syndrome (MPS-IV)
- Maroteaux-Lamy Syndrome (MPS-VI)
- Sly Syndrome, Beta-Glucuronidase Deficiency (MPS-VII)
- Adrenoleukodystrophy
- Mucolipidosis II (I-cell Disease)
- Krabbe Disease
- Gaucher's Disease
- Niemann-Pick Disease
- Wolman Disease
- Metachromatic Leukodystrophy
Histiocytic Disorders (4)
- Familial Erythrophagocytic Lymphohistiocytosis
- Histiocytosis-X
- Hemophagocytosis
Inherited Immune System Disorders (13)
- Ataxia-Telangiectasia
- Kostmann Syndrome
- Leukocyte Adhesion Deficiency
- DiGeorge Syndrome
- Bare Lymphocyte Syndrome
- Omenn's Syndrome
- Severe Combined Immunodeficiency (SCID)
- SCID with Adenosine Deaminase Deficiency
- Absence of T & B Cells SCID
- Absence of T Cells, Normal B Cell SCID
- Common Variable Immunodeficiency
- Wiskott-Aldrich Syndrome
- X-Linked Lymphoproliferative Disorder
Other Inherited Disorders (4)
- Lesch-Nyhan Syndrome
- Cartilage-Hair Hypoplasia
- Glanzmann Thrombasthenia
- Inherited Platelet Abnormalities
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