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MUMS:  List of Disorders I - J  Number in parentheses indicates number of matches. * indicates there is a support group which covers that diagnosis.

• I-Cell Disease (Mucolipidosis Type II) (8) *
• IGA Deficiency (8)*
• IGA Linear Bollos Dermatitis (1)
• IGA Nephropathy (1)*
• IGG Deficiency (1)*
• IGG Subclass Deficiency (2) *
• IGG2 Deficiency (1)*
• Ichthyosis (14) **
• Ichthyosis Linear Circumflexa (Netherton ) (3)
• Ichthyosis, Collodian Membrane (ichthyosiform Erthrodermia) (2) *
• Ichthyosis, Epidermolytic Hyperkeratosis (4) *
• Ichthyosis, Follicularis w/Alopecia & Photopholia (1)*
• Ichthyosis, Lamellar (7) *
• Ichthyosis, Netherton Syndrome (3) *
• Ichthyosis, Sjogren Larsson Syndrome (1)*
• Ichthyosis, X-Linked (1) *
• Ideopathic Systemic Capillary Leak Syndrome (1)
• Idiopathic Hypertrophic Subaortic Stenosis (IHSS) (3) *
• Idiopathic Thrombocytopenia Purpura (ITP) (19)**
• Ileostomy (7)
• Immeyer's Association (1)
• Immotile Cilia Syndrome (Kartagener) (15)
• Immune Deficiency (151) *
• Immune Deficiency, Subclass 3 Level Low C4 Compliment (1)
• Immunoglobin Type A Deficiency (1)
• Immunodeficiency, Agranulocytosis Kostmann Type (3)
• Immunodeficiency, Common Variable Type (4)
• Immunodeficiency, Reticuloendotheliosis with Eosinophilia (1) *
• Imperforate Anuc & Celiac Sprue (1)
• Imperforate Anus (no anal opening) (87) **
• Incontinentia Pigmenti (24) **
• Incontinentia Pigmenti & Cerebral Palsy (3)
• Independent Familial Precocious Puberty (1)*
• Infantile Fascioscapuloperoneal Dystrophy (1)
• Infantile Fibromatosis (tumor in submandular gland) (1)
• Infantile Fibrosarcoma (1)
• Infantile Hypercalcaemia (Williams Syndrome) (40)**
• Infantile Myofibromitosis (1)
• Infantile Neuroaxonal Dystrophy (5)*
• Infantile Spasms (167) *
• Infantile Spinal Muscular Atrophy (Werdnig-Hoffman) (24) **
• Inflammatory Bowel Disease (1)
• Innate Laryngeal Cartilage Hypoplasia (1)
• Intermittent Explosive Disorder (10)
• Intestinal Hypoperistalsis Syndrome (megacystis, microcolon) (5)
• Intestinal Lymphangiectasia (14)*
• Intestinal Neuronal Dysplasia (3)*
• Intestinal Pseudobstruction (7) *
• Intestional Malrotation (19)
• Intestinal Webs, Multiple Non-Duodenal (1)
• Intrahepatic Biliary Artresia or Dysgenesis (Alagile Syndrome) (12) *
• Intrauterine Growth Deficiency (24) *
• Intraventricular Hemorrhage (IVH) (45) *
• Intraventricular Hemorrhage (brain bleed) Grade II (3) *
• Intraventricular Hemorrhage (brain bleed) Grade III (5) *
• Intraventricular Hemorrhage (brain bleed) Grade IV (19) *
• Iritis (inflammation of front portion of the eye) (3)
• Iron Lung (1)
• Irritable Bowel Syndrome (3) *
• Isochromosome Yp w/deletion Yq- (1)
• Isolated Antibody Deficiency & Pneumoccocal Hepatitis (1)
• Isolated Sulfite Oxidase Deficiency (1)
• Isotretinoin Embryopathy (1) www.xsorbit1.com/usets/itrembryopathy/index.cgi
• Isovaleric Acidaemia (4) *
• Ivemark Syndrome (Right Atrial Isomerism & absent spleen) (6)*

• Jacobsen's Syndrome (7)*
• Jaffe-Litchenstein Disease (1)
• Jarcho-Levin Syndrome (Spondylothoracic Dysplasia) (2)
• Jaundice (25)
• Jaundice, Chronic Undiagnosed (1)
• Jaundice, Untreated (2)
• Jaw-Winking (Marcus Gunn Phenomenon) (3)
• Jejunal Atresia (3)
• Jejunal Interposition (1)
• Jejunal-Tube for Feeding (32)
• Jeune Syndrome (12) **
• Job Syndrome (Hyper IGE Type Immunodeficiency (5)
• Johanson-Blizzard Syndrome (3) *
• Joints, Osteochondritis Dissecans (Kohler Disease) (1)
• Joubert Syndrome (12) *