Madisons Foundation - Moms And Dads In Search Of Needed Support

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Your Child's Disease Information

Disease --- Select from the m-Power Database --- --- Not listed in the m-Power Database --- 3-M Syndrome Aarskog Syndrome Aase Syndrome Aberrant Subclavian Artery Abetalipoproteinemia Achondrogenesis Type I Achondroplasia Achromatopsia Acoustic Neuroma Acquired Cold Urticaria Acrodermatitis Enteropathica Acute Disseminated Encephalomyelitis (ADEM) Acute Intermittent Porphyria Acute Lymphoblastic Leukemia (ALL) Adult-Type Fibrosarcoma (ATFS) Agammaglobulinemia, X-linked (XLA) Agenesis of the Corpus Callosum Aicardi Syndrome Alagille Syndrome Alagille Syndrome (AGS) Albinism Alexander Disease Alexander Disease Alkaptonuria Allergic Bronchopulmonary Aspergillosis (ABPA) Alpers' Disease Alpha and Beta Thalassemia Alpha-1-Antitrypsin Deficiency Alpha-Mannosidosis Alport Syndrome Alström Syndrome Alveolar Soft-Part Sarcoma (ASPS) Ambiguous Genitalia Androgen Insensitivity Syndrome (AIS) Angelman Syndrome Angiomatoid Malignant Fibrous Histiocytoma (AMFH) Angiosarcoma Antiphospholipid Antibody Syndrome Apert Syndrome Aplasia Cutis Congenita Aplastic Anemia Argininemia Argininosuccinic Aciduria (ASA) Arnold Chiari Malformation (ACM) Arthrogryposis Aspartylglycosaminuria Astrocytoma Ataxia Telangiectasia (AT) Atrial Myxoma Autistic Disorder Autoimmune Hemolytic Anemia Autoimmune Lymphoproliferative Syndrome (ALPS) Autoimmune Polyglandular Syndrome Autosomal Recessive Polycystic Kidney Disease Barakat Syndrome Bardet-Biedl Syndrome (BBS) Bare Lymphocyte Syndrome Bartter syndrome Basilar Invagination Batten Disease Beals Syndrome Becker Muscular Dystrophy (BMD) Beckwith-Wiedemann Syndrome (BWS) Behcet's Disease Behcet's Disease (BD) Bell's Palsy Benign Familial Hematuria Benign Familial Neonatal Seizures Bernard-Soulier Syndrome Biliary Atresia Biotinidase Deficiency Bladder Exstrophy Bloom Syndrome Budd-Chiari Syndrome Byler's Disease Caffey Disease Canavan Disease Carbamoyl Phosphate Synthetase One Deficiency Carney Complex Caroli Disease Cartilage-Hair Hypoplasia Castleman's Disease Cat Eye Syndrome (CES) Celiac Disease Cerebral Cavernous Malformation Chagas Disease Char Syndrome Charcot-Marie-Tooth-Disease CHARGE Syndrome Chediak-Higashi Syndrome (CHS) Cherubism Chondroectodermal Dysplasia Chondrosarcoma Chronic Granulomatous Disease (CGD) Chronic Inflammatory Demyelinating Polyneuropathy Churg Strauss Syndrome Citrullinemia Coarctation of the Aorta Cockayne Syndrome Coffin-Lowry Syndrome (CLS) Coffin-Siris Syndrome Cogan Syndrome Cohen Syndrome Common Variable Immunodeficiency (CVID, CVI) Complement Deficiencies Complete Transposition of the Great Arteries Complex Regional Pain Syndrome (CRPS) Congenital Adrenal Hyperplasia Congenital Atransferrinemia Congenital Bronchobiliary Fistula Congenital Contractural Arachnodactyly Congenital Cystic Adenomatoid Malformation Congenital Diaphragmatic Hernia Congenital Fibrosarcoma Congenital Hepatic Fibrosis (CHF) Congenital Ichthyosis Erythroderma Congenital Parvovirus B19 Infection Congenital Sideroblastic Anemia Congenital Sucrase-Isomaltase Deficiency Cornelia de Lange Syndrome (CdLS) Costello Syndrome Cowden Disease Craniopharyngioma Cri-du-chat Syndrome Crigler-Najjar Syndrome (CNS) Crohn's Disease Cronkhite-Canada Syndrome Crouzon Syndrome Cutaneous Polyarteritis Nodosa (CPN) Cutis Laxa Cyclic Neutropenia Cyclic Vomiting Syndrome Cystic Fibrosis (CF) Cystinosis Cystinuria Dandy-Walker Syndrome (DWS) De Jerine-Sottas Disease De Morsier Syndrome Desmoid Tumors Diamond-Blackfan Anemia (DBA) Diaphyseal Dysplasia Diencephalic Syndrome DiGeorge Syndrome DiGeorge Syndrome Disseminated Intravascular Coagulopathy (DIC) Dubin-Johnson Syndrome Dubowitz Syndrome Duchenne Muscular Dystrophy Dysautonomia Dyskeratosis Congenita (DC) Ebstein's Anomaly Ectodermal Dysplasia (ED) Ehlers-Danlos Syndrome (EDS) Emery-Dreifuss Syndrome Endocardial Fibroelastosis Eosinophilia Myalgia Syndrome (EMS) Eosinophilic Cystitis (EC) Eosinophilic Fasciitis Eosinophilic Gastroenteritis Eosinophilic Pneumonia (EP) Ependymoma Epidermolysis Bullosa (hemidesmosomal epidermolysi Episodic angioedema with eosinophilia Epithelioid sarcoma Evan's Syndrome Ewing's Sarcoma (ES) Exercise-Induced Anaphylaxis (EIA) Fabry Disease Facioscapulohumeral Muscular Dystrophy Factor V Deficiency Factor X Deficiency Factor XII Deficiency Factor XIII Deficiency Familial Adenomatous Polyposis (FAP) Familial Cold Urticaria Familial Hemophagocytic Lymphohistiocytosis Familial Hyperinsulinism (FHI) Familial Mediterranean Fever (FMF) Familial Paroxysmal Choreoathetosis Fanconi Anemia (FA) Farber Disease Fetal Alcohol Syndrome (FAS) FG syndrome Fibroma Fibromatosis Fibromyalgia Syndrome (FMS) Fibrous Dysplasia Fibrous Hamartoma of Infancy (FHI) Fibrous Histiocytoma Fifth Disease Fragile X Syndrome Free Sialic Acid Storage Disease Freeman Sheldon Syndrome Friedreich Ataxia Fructose 1,6-Diphosphatase Deficiency Fryns Syndrome Fucosidosis G-6-PD Deficiency (G-6-PD) Galactosemia Gardner Syndrome Gaucher Disease Gilbert Syndrome Glutaric Acidemia Type I Glycogen Storage Disease Type 1a (GSD 1) Glycogen Storage Disease Type 1B Glycogen Storage Disease Type V Glycogen Storage Disease, Type 0 Glycogen Storage disease: Type 3 Glycogen-Storage Disease Type VI Goldenhar Syndrome Goodpasture's Syndrome Gorham Stout Disease (GSD) Gorlin Syndrome Greig Cephalopolysyndactyly Syndrome Growth Hormone Deficiency Guillain-Barre Syndrome Hajdu-Cheney Hallermann Streiff Syndrome Hartnup Disease Hawkinsinuria Heiner Syndrome Hemihypertrophy Hemochromatosis Hemoglobin C Disease Hemoglobin H Disease Hemolytic Uremic Syndrome Hemophilia (A and B) Henoch-Schonlein Purpura (HSP) Hepatitis B Hepatitis C Hepatitis D Hepatitis E Virus (HEV) Hepatoblastoma Hereditary Angioedema (HAE) Hereditary Orotic Aciduria Hereditary Spherocytosis (HS) Hereditary Tyrosinemia Hermansky-Pudlak Syndrome Heterotaxy Syndrome Hidrotic Ectodermal Dysplasia (HED) Hirschsprung Disease Hodgkin's Disease Holoprosencephaly Holt Oram Syndrome Homocystinuria Hunter Syndrome Huntington Disease Hurler Syndrome Hyper IgD Syndrome (HIDS) Hyper IgE Syndrome Hyper IgM Hyperoxaluria, Primary, Type 1 Hypersensitivity Vasculitis Hypohidrotic Ectodermal Dysplasia Hypophosphatemic Rickets, X-Linked Hypoplastic Left Heart Syndrome (HLHS) Hypothalamic Hamartoma Ichthyosis Vulgaris Idiopathic Pulmonary Hemosiderosis Idiopathic Thrombocytopenic Purpura IgG Subclass Deficiencies Incontinentia Pigmenti Intracranial Germinomas Isaac's Syndrome Isovaleric Acidemia Jarcho-Levin Syndrome Jervell and Lange-Nielsen Syndrome Jeune's Syndrome Johanson-Blizzard Syndrome Joubert Syndrome Juvenile Angiofibroma Juvenile Ankylosing Spondylitis (JAS) Juvenile Dermatomyositis Juvenile Myelomonocytic Leukemia (JMML) Juvenile Parkinson's Disease Juvenile Polyposis Syndrome Juvenile Rheumatoid Arthritis (JRA) Kabuki Syndrome Kallmann's Syndrome Kartagener Syndrome (KS) Kasabach-Merritt Syndrome Kawasaki Syndrome (KS) Kearns-Sayre Syndrome Kikuchi Syndrome Klinefelter Syndrome Klippel-Feil Syndrome Klippel-Trenaunay-Weber Syndrome (KTWS) Kohlmeier-Degos Syndrome Kostmann's Agranulocytosis Krabbe Disease Krause Kivlin Syndrome Kugelberg-Welander Spinal Muscular Atrophy Lafora Disease Lamellar Ichthyosis Landau-Kleffner Syndrome Langer-Giedion Syndrome Laurence-Moon Syndrome Lead Poisoning Leigh Disease Leiner's Disease Lennox-Gastout Syndrome (LGS) Lenz Microphthalmia Syndrome LEOPARD syndrome Lesch-Nyhan Syndrome Lichen Planus (LP) Lissencephaly Long-Chain Acyl-CoA Dehydrogenase Deficiency Lowe Syndrome Lown-Ganong-Levine Syndrome Lyme Disease Lymphangiectasia Löffler's Syndrome Machado-Joseph Disease Maffucci Syndrome Malignant Hyperthermia Maple Syrup Urine Disease Marden-Walker Syndrome Marfan Syndrome (MS) Marinesco-Sjogren syndrome Mastocytosis May-Hegglin Anomaly McCune-Albright Syndrome Meckel-Gruber Syndrome (MKS) Medium-Chain Acyl-CoA Dehydrogenase Deficiency Medulloblastoma Megaloblastic Anemia MELAS Menetrier's Disease Meningioma Menkes Disease (Syndrome) Metachromatic Leukodystrophy Metatropic dysplasia Methemoglobinemia Miller Syndrome and Nager Syndrome Miller-Dieker Syndrome Mixed Connective Tissue Disease (MCTD) Moebius Syndrome Morquio Syndrome Moyamoya Disease Moyamoya Disease Mucha-Habermann Syndrome Muckle-Wells Syndrome Mucolipidosis IV Mucolipidosis Type 1 Mucopolysaccharidoses Multiple Epiphyseal Dysplasia (MED) Multiple Sclerosis (MS) Multiple System Atrophy Myasthenia Gravis Myeloperoxidase Deficiency Myoclonic Epilepsy Associated with Ragged-Red Fibe Myofibrosarcoma Myotonic Dystrophy Myotubular myopathy NAGS Deficiency Nail-Patella Syndrome Neonatal Hepatitis Neonatal Onset Multisystem Inflammatory Disease Nephrogenic Diabetes Insipidus Neuroblastoma (NB) Neurofibroma Plexiform Tumors Neurofibromatosis type 1 (NF1) Neurofibromatosis Type 2 (NF2) Nezelof Syndrome Niemann-Pick Disease (types A,B,C,D) Nijmegen Breakage Syndrome Non-Hodgkin's Lymphoma (NHL) Noonan Syndrome Norrie Disease Occipital Horn Syndrome (OHS) Omenn's Syndrome Optic Nerve Glioma Oral Facial Digital Syndrome Type I Ornithine Transcarbamylase Deficiency (OTC) Osler-Weber-Rendu Syndrome Osteochondritis Dissecans Osteogenesis Imperfecta (OI) Osteoid Osteoma Osteosarcoma Pallister-Hall Syndrome Pallister-Killian Syndrome Pancreatitis Pandas Syndrome Pantothenate Kinase-Associated Neurodegeneration Paraneoplastic Limbic Encephalitis Paroxysmal Nocturnal Hemoglobinuria (PNH) Pearson's Syndrome Pelizaeus-Merzbacher Disease Pena-Shokeir Syndrome, Type I Pendred Syndrome Peutz-Jeghers Syndrome PFAPA Syndrome Pfeiffer Syndrome Phenylketonuria Phenylketonuria (PKU) Pheochromocytoma Pierre Robin Sequence Pilocytic Astrocytoma Poland Syndrome Polyarteritis Nodosa (PAN) Polycythemia Vera Polyglandular Autoimmune Syndrome, Type 1 Pompe Disease Potter's Syndrome Prader-Willi Syndrome Primary Angiitis Primary Lymphangiomatosis Progeria Progressive Multifocal Leukoencephalopathy (PML) Progressive Rubella Panencephalitis (PRP) Propionic Acidemia (PA) Protein Losing Enteropathy (PLE) Proteus Syndrome Prune Belly Syndrome Pseudotumor Cerebri Pseudoxanthoma Elasticum Pulmonary Hypertension Pyruvate Decarboxylase Deficiency Pyruvate Kinase Deficiency (PKD) Rasmussen's Encephalitis (RE) Refsum Disease Reiter's Syndrome (RS) Relapsing Panniculitis Relapsing Polychondritis (RP, RPC) Retinoblastoma Rett Syndrome Reye's Syndrome Rhabdomyosarcoma Ring Chromosome 14 Syndrome (r14, Ring 14) Robinow Syndrome Romano-Ward Syndrome Rothmund-Thomsun Syndrome Roussy-Levy Syndrome Rubinstein-Taybi Syndrome Rubinstein-Taybi Syndrome (RTS) Russell-Silver Syndrome (RSS) Saethre-Chotzen Syndrome Sandhoff Disease Sanfilippo Syndrome Sarcoidosis Scheie syndrome Schindler Disease Schizencephaly Schizencephaly Schnitzler's Syndrome Schwannomatosis Scleroderma Selective IgA Deficiency Selective Immunoglobulin M Deficiency (SIgMD) Severe Combined Immunodeficiency (SCID) Shone's Complex Short Chain Acyl CoA Dehydrogenase Deficiency (SCA Short Rib-Polydactyly Syndrome I-IV Shwachman-Diamond Syndrome (SDS) Sickle Cell Anemia Sirenomelia Syndrome Sjögren's Syndrome Smith Lemli Opitz Syndrome (SLOS) Smith-Magenis Syndrome Smith-Magenis Syndrome Soft-Tissue Angiomatosis Sotos Syndrome Spina Bifida Spinal Muscular Atrophy (SMA) Spondyloepiphyseal Dysplasia Congenita Stevens-Johnson Syndrome Stickler Syndrome Sturge-Weber Syndrome (SWS) Subacute Sclerosing Panencephalitis (SSPE) Sulfite Oxidase Deficiency Sweet Syndrome Syringomyelia Systemic Lupus Erythematosus Tarui Disease Tay-Sachs Disease (TSD) Telogen Effluvium Tethered Cord Syndrome Tetralogy of Fallot (TOF) Tetrasomy X Thanatophoric Dysplasia Thrombocytopenia Absent Radii (TAR) Syndrome Total Anomalous Pulmonary Venous Return (TAPVR) Tourette Syndrome Townes-Brocks Syndrome Transient Erythroblastopenia of Childhood (TEC) Transient Familial Neonatal Hyperbilirubinemia Transient Hypogammaglobulinemia of Infancy (THI) Treacher Collins Syndrome (TCS) Trichorhinophalangeal Syndrome Type II Trimethylaminaria Trimethylaminuria Trisomy 13 Trisomy 18 Trisomy 21 Trisomy 8 Trisomy X Truncus Arteriosus Tuberous Sclerosis Turcot's Syndrome Turner Syndrome (TS) Turner Syndrome (TS) Ulcerative Colitis Unverricht-Lundburg Disease Usher Syndrome Von Hippel-Lindau Disease Von Willebrand Disease (vWD) Waardenburg Syndrome (WS) Waldenstrom's Macroglobulinemia (WM) Weaver Syndrome Wegener's Granulomatosis Wells Syndrome Werdnig-Hoffman Disease Werner's Syndrome West Syndrome Whipple's Disease Wildervanck Syndrome Williams Syndrome Wilms' Tumor (WT) Wilsons Disease Wiskott-Aldrich Syndrome (WAS) Wolf-Hirschhorn Syndrome (WHS) Wolman Disease X-Linked Ichthyosis Xeroderma Pigmentosum Young Onset Parkinson's Disease (YOPD) Zellweger Syndrome

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