Diseases List: I
List of diseases with information available on this website:
- I cell disease
- Iatrogenic Disorder
- Ibuprofen response
- Ice-cream headache
- ICF syndrome
- Ichthyosiform erythroderma, corneal involvement, deafness
- Ichthyosis
- Ichthyosis alopecia eclabion ectropion mental retardation
- Ichthyosis bullosa of Siemens
- Ichthyosis cheek eyebrow syndrome
- Ichthyosis congenita biliary atresia
- Ichthyosis follicularis atrichia photophobia syndrome
- Ichthyosis hystrix gravior
- Ichthyosis hystrix, Curth Macklin type
- Ichthyosis lamellar
- Ichthyosis lamellar type 1
- Ichthyosis lamellar type 2
- Ichthyosis lamellar type 3
- Ichthyosis lamellar, autosomal dominant
- Ichthyosis prematurity syndrome
- Ichthyosis tapered fingers midline groove up
- Ichthyosis vulgaris
- Ichthyosis with confetti
- Ichthyosis with hypotrichosis, autosomal recessive
- Ichthyosis, acquired
- Ichthyosis, congenital, autosomal recessive type 11
- Ichthyosis, cyclic, with epidermolytic hyperkeratosis
- Ichthyosis, follicular
- Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
- Ichthyosis, mental retardation, dwarfism and renal impairment
- Ichthyosis, spastic quadriplegia, and mental retardation
- Ichthyosis-mental retardation syndrome with large keratohyalin granules in the skin
- Ideational apraxia
- Idiopathic
- Idiopathic achalasia
- Idiopathic acute eosinophilic pneumonia
- Idiopathic alveolar hypoventilation syndrome
- Idiopathic angioedema
- Idiopathic aortitis
- Idiopathic basal ganglia calcification childhood-onset
- Idiopathic basal ganglia calcification type 1
- Idiopathic basal ganglia calcification type 5
- Idiopathic Bronchiectasis
- Idiopathic CD4 lymphocytopenia
- Idiopathic CD4 positive T-lymphocytopenia
- Idiopathic edema
- Idiopathic fatigue
- Idiopathic fibrosing alveolitis, chronic form
- Idiopathic gastroparesis
- Idiopathic generalized epilepsy
- Idiopathic guttate hypomelanosis
- Idiopathic hypercalcemia of infancy
- Idiopathic hypereosinophilic syndrome
- Idiopathic hypersomnia
- Idiopathic Hypersomnolence
- Idiopathic inflammatory myopathy
- Idiopathic Interstitial Pneumonia
- Idiopathic Intracranial Hypertension
- Idiopathic Juvenile Osteoporosis
- Idiopathic juxtafoveal retinal telangiectasia
- Idiopathic livedo reticularis with systemic involvement
- Idiopathic myopathy
- Idiopathic neutropenia
- Idiopathic obesity
- Idiopathic precocious puberty
- Idiopathic Pulmonary Fibrosis
- Idiopathic pulmonary hemosiderosis
- Idiopathic scoliosis
- Idiopathic spinal cord herniation
- Idiopathic thrombocytopenic purpura
- IFAP syndrome with or without BRESHECK syndrome
- IgA deficiency
- IgA glomerulonephritis
- IgA nephropathy
- IgA pemphigus
- IgA vasculitis
- IgE deficiency
- Ige responsiveness, atopic
- IgG deficiency
- IgG4-related disease
- IgM deficiency
- Iida Kannari syndrome
- IL12RB1 deficiency
- IL21R immunodeficiency
- Ileal Band
- Ileal Carcinoid Tumor
- Ileal Diseases
- Ileal Fistula
- Ileal Hemorrhage
- Ileal Neoplasm
- Ileal Obstruction
- Ileal Perforation
- Ileal pouch anal anastomosis related faecal incontinence
- Ileal Stenosis
- Ileal Ulcer
- Ileal Web
- Ileitis
- Ileostomy
- Ileum cancer
- Ileum tumor
- Ileus
- Iliac crest serration
- Iliotibial Band Syndrome
- Ilium Fracture
- IMAGe syndrome
- Imaizumi Kuroki syndrome
- Imatinib response
- Imbalanced hemoglobin synthesis
- Imerslund-Grasbeck syndrome
- Imerslund-Gräsbeck syndrome
- Iminoglycinuria
- Imipramine response
- Immature Extragonadal Teratoma
- Immature Gastric Teratoma
- Immature Granulocytic Sarcoma
- Immature Mediastinal Teratoma
- Immature Ovarian Teratoma
- Immature Retinal Vasculature
- Immature Retinopathy of Prematurity
- Immature Teratoma
- Immature Testicular Teratoma
- Immediate Hypersensitivity
- Immersion foot
- Immotile cilia syndrome, due to defective radial spokes
- Immune Cell Cancers
- Immune Complex Glomerulonephritis
- Immune Complex Mediated Membranoproliferative Glomerulonephritis
- Immune defect due to absence of thymus
- Immune deficiency
- Immune Deficiency Disorders
- Immune Disorders
- Immune dysfunction with T-cell inactivation due to calcium entry defect type 1
- Immune dysfunction with T-cell inactivation due to calcium entry defect type 2
- Immune Dysregulation Polyendocrinopathy and Enteropathy X-linked Syndrome
- Immune dysregulation, polyendocrinopathy, enteropathy, X-linked
- Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome
- Immune Hemolytic Anemia
- Immune Hydrops Fetalis
- Immune Reconstitution Inflammatory Syndrome
- Immune Reconstitution Inflammatory Syndrome Associated with Kaposi Sarcoma
- Immune System Disorders
- Immune Thrombocytopenia
- Immune-mediated thrombocytopenia
- Immunoblastic Lymphoma
- Immunoblastic Lymphoma PTLD
- Immunodeficiency
- Immunodeficiency due to defect in cd3-epsilon
- Immunodeficiency due to defect in CD3-gamma
- Immunodeficiency due to defect in cd3-zeta
- Immunodeficiency due to defect in mapbp-interacting protein
- Immunodeficiency due to ficolin 3 deficiency
- Immunodeficiency of Unknown Origin
- Immunodeficiency type 11
- Immunodeficiency type 12
- Immunodeficiency type 13
- Immunodeficiency type 14
- Immunodeficiency type 15
- Immunodeficiency type 16
- Immunodeficiency type 17
- Immunodeficiency type 18
- Immunodeficiency type 19
- Immunodeficiency type 20
- Immunodeficiency type 22
- Immunodeficiency type 24
- Immunodeficiency type 26 with or without neurologic abnormalities
- Immunodeficiency type 27b
- Immunodeficiency type 28
- Immunodeficiency type 29
- Immunodeficiency type 30
- Immunodeficiency type 31a
- Immunodeficiency type 31C
- Immunodeficiency type 32a
- Immunodeficiency type 32b
- Immunodeficiency type 36
- Immunodeficiency type 38 with basal ganglia calcification
- Immunodeficiency type 8
- Immunodeficiency with hyper IgM type 1
- Immunodeficiency with hyper IgM type 2
- Immunodeficiency with hyper IgM type 3
- Immunodeficiency with hyper IgM type 4
- Immunodeficiency with hyper IgM type 5
- Immunodeficiency with hyper-IgM
- Immunodeficiency with thymoma
- Immunodeficiency without anhidrotic ectodermal dysplasia
- Immunodeficiency, common variable, type 12
- Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia
- Immunodeficiency-centromeric instability-facial anomalies syndrome
- Immunodeficiency-centromeric instability-facial anomalies syndrome type 2
- Immunodeficiency-Related Burkitt's Lymphoma
- Immunodeficiency-Related Disorder
- Immunodeficiency-Related Malignant Neoplasm
- Immunodeficiency-Related Neoplasm
- Immunodysregulation, polyendocrinopathy and enteropathy X-linked
- Immunoglobulin A deficiency
- Immunoglobulin A deficiency type 1
- Immunoglobulin A deficiency type 2
- Immunoglobulin Deposition
- Immunoglobulin G deficiency
- Immunoglobulin Heavy Chain Deletion
- Immunoglobulin IgG2 deficiency
- Immunoglobulin kappa light chain deficiency
- Immunoglobulin m, level of
- Immunoglobulin Superfamily Member 1 Deficiency Syndrome
- Immunoosseous Dysplasia, Schimke Type
- Immunosuppression
- Immunosuppression-Related Post-Transplant Toxicity
- Immunosuppressive Therapy-related Kaposi Sarcoma
- Immunotactoid glomerulopathy
- Immunotactoid or fibrillary glomerulopathy
- Immunotoxicity
- Impacted cerumen
- Impacted teeth, multiple
- Impacted Tooth
- Impaired ADP-induced platelet aggregation
- Impaired distal proprioception
- Impaired distal tactile sensation
- Impaired distal vibration sensation
- Impaired fasting glucose
- Impaired Fertility
- Impaired horizontal smooth pursuit
- Impaired left ventricular function
- Impaired ocular abduction
- Impaired ocular adduction
- Impaired pain sensation
- Impaired platelet aggregation
- Impaired proprioception
- Impaired renal concentrating ability
- Impaired smooth pursuit
- Impaired T cell function
- Impairment of oral perception
- Impalement injuries
- Imperforate anus
- Imperforate Hymen
- Imperforate oropharynx-costo vetebral anomalies
- Imperforate Vagina
- Impetigo
- Implant Failure
- Implantation Bleeding
- Implantation Failure
- Impotence
- Impulse Control Disorders
- Impulsivity Disorders
- In Situ Lesion
- In Stent Restenosis
- In Utero Bowel Perforation
- In Utero Drug Exposure
- In-utero Drug Withdrawal
- Inappropriate ADH Syndrome
- Inappropriate Antidiuretic Hormone Secretion Syndrome
- Inappropriate Manual Collimation
- Inappropriate Sinus Tachycardia
- Inattention Disorders
- Inborn amino acid metabolism disorder
- Inborn Amino Acid Transport Disorders
- Inborn errors in primary bile acid synthesis
- Inborn Errors of Lipid Metabolism
- Inborn Errors of Metabolism
- Inborn Genetic Diseases
- Inborn Urea Cycle Disorder
- Incarcerated Hernia
- Incarcerated Inguinal Hernia
- Incident Nephrotic Syndrome
- Incisional Burn
- Incisional Hernia
- Inclusion Body
- Inclusion body myopathy 2
- Inclusion body myopathy type 3
- Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
- Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporaldementia
- Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1
- Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia type 2
- Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia type 3
- Inclusion body myositis
- Inclusion Conjunctivitis
- Inclusion-Like Nucleoli
- Incompetent Cervix
- Incomplete Abortion
- Incomplete Bundle Branch Block
- Incomplete Chondrogenesis
- Incomplete Laryngeal Vestibular Closure
- Incomplete Left Bundle Branch Block
- Incomplete Maternal Surface of Placenta
- Incomplete Ossification
- Incomplete partition of the cochlea type II
- Incomplete Pharyngeal Contraction
- Incomplete Protocol Artifact
- Incomplete Right Bundle Branch Block
- Incontinence
- Incontinent Epispadias
- Incontinentia pigmenti
- Incontinentia pigmenti achromians
- Incontinentia pigmenti syndrome
- Increased CSF interferon alpha
- Increased CSF lactate
- Increased CSF protein
- Increased inflammatory response
- Increased jitter at single fibre EMG
- Increased rate of premature chromosome condensation
- Increased vertebral height
- Indifference to pain, congenital, autosomal recessive
- Indirect inguinal hernias
- Indolent B cell lymphoma
- Indolent mastocytosis
- Indolent non-Hodgkin's lymphoma
- Indolent Systemic Mastocytosis
- Induced Cataract
- Inducible Myocardial Ischemia
- Infant Colic
- Infant dental disorders
- Infant disorders
- Infant Leukemia
- Infant Nutrition Disorders
- Infant reflux
- Infant Respiratory Distress Syndrome
- Infant sticky eye
- Infant tooth decay
- Infantile apnea
- Infantile axial hypotonia
- Infantile axonal neuropathy
- Infantile cataracts
- Infantile cerebellar-retinal degeneration
- Infantile choriocarcinoma of the liver
- Infantile convulsions and paroxysmal choreoathetosis, familial
- Infantile cortical hyperostosis
- Infantile digital fibromatosis
- Infantile eczema
- Infantile encephalopathy
- Infantile epileptic encephalopathy
- Infantile fibrosarcoma
- Infantile free sialic acid storage disease
- Infantile Gastrointestinal Reflux
- Infantile GM1 gangliosidosis
- Infantile Hemangioendothelioma
- Infantile Hemangioma
- Infantile hemangiopericytoma
- Infantile histiocytoid cardiomyopathy
- Infantile hypophosphatasia
- Infantile liver failure syndrome
- Infantile liver failure syndrome type 1
- Infantile liver failure syndrome type 2
- Infantile Melanotic Neuroectodermal Neoplasm
- Infantile muscular hypotonia
- Infantile myofibromatosis
- Infantile myofibromatosis type 1
- Infantile myofibromatosis type 2
- Infantile NCL
- Infantile nephronophthisis
- Infantile Neuroaxonal Dystrophy
- Infantile neuronal ceroid lipofuscinosis
- Infantile nystagmus, X-linked
- Infantile Parkinsonism-dystonia
- Infantile recurrent chronic multifocal osteomyolitis
- Infantile Refsum Disease
- Infantile Scurvy
- Infantile Sialic Acid Storage Disorder
- Infantile Spasms
- Infantile spasms broad thumbs
- Infantile systemic hyalinosis
- Infantile-onset ascending hereditary spastic paralysis
- Infantile-onset spinocerebellar ataxia
- Infantile-onset X-linked spinal muscular atrophy
- Infarction
- Infected pancreatic necrosis
- Infected pilonidal sinus
- Infection
- Infection-associated hemolytic uremic syndrome
- Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations
- Infectious Arteritis
- Infectious Arthritis
- Infectious Bone Diseases
- Infectious Bovine Rhinotracheitis
- Infectious Cervicitis
- Infectious Colitis
- Infectious Conjunctivits
- Infectious Cystitis
- Infectious dermatitis
- Infectious Diarrhea
- Infectious diseases
- Infectious Encephalitis
- Infectious Encephalomyelitis
- Infectious Enterocolitis
- Infectious Gastroenteritis
- Infectious Granuloma
- Infectious Hidradenitis
- Infectious Keratitis
- Infectious Lung Disorder
- Infectious Mediastinitis
- Infectious Meningitis
- Infectious Otitis Media
- Infectious Rhinitis
- Infectious Salpingitis
- Infectious Skin Diseases
- Infectious thyroiditis
- Infectious-Mononucleosis-Like PTLD
- Infective endocarditis
- Infective mastitis
- Infective Myositis
- Infective Phlebitis
- Inferior Myocardial Infarction
- Inferior Vena Cava Leiomyosarcoma
- Inferior Vena Cava Occlusion
- Inferior Vena Cava Stenosis
- Inferolateral Myocardial Infarction
- Infertility
- Infertility associated with multi-tailed spermatozoa and excessive DNA
- Infertility due to oligospermia
- Infestations
- Infiltrating Angiolipoma
- Infiltrating Basal Cell Carcinoma
- Infiltrating Bladder Lymphoepithelioma-like Carcinoma
- Infiltrating Bladder Urothelial Carcinoma Associated with Urethral Carcinoma
- Infiltrating Bladder Urothelial Carcinoma Clear Cell Variant
- Infiltrating Bladder Urothelial Carcinoma Lipid Cell Variant
- Infiltrating Bladder Urothelial Carcinoma Lymphoma-like Variant
- Infiltrating Bladder Urothelial Carcinoma Microcystic Variant
- Infiltrating Bladder Urothelial Carcinoma Nested Variant
- Infiltrating Bladder Urothelial Carcinoma Plasmacytoid Variant
- Infiltrating Bladder Urothelial Carcinoma Sarcomatoid Variant
- Infiltrating Bladder Urothelial Carcinoma Sarcomatoid Variant with Heterologous Elements
- Infiltrating Bladder Urothelial Carcinoma Sarcomatoid Variant without Heterologous Elements
- Infiltrating Bladder Urothelial Carcinoma with Giant Cells
- Infiltrating Bladder Urothelial Carcinoma with Glandular Differentiation
- Infiltrating Bladder Urothelial Carcinoma with Squamous Differentiation
- Infiltrating Bladder Urothelial Carcinoma with Trophoblastic Differentiation
- Infiltrating Cervical Carcinoma
- Infiltrating Ductal and Lobular Carcinoma in situ
- Infiltrating Intramuscular Lipoma
- Infiltrating Lipoma
- Infiltrating Papillary Adenocarcinoma
- Infiltrating Renal Pelvis and Ureter Urothelial Carcinoma
- Infiltrating Tumor Margins Present
- Infiltrating Urothelial Carcinoma
- Inflammation
- Inflammatory abnormality of the eye
- Inflammatory arthritis
- Inflammatory Bowel Disease
- Inflammatory Bowel Disease in Children
- Inflammatory bowel disease type 1
- Inflammatory bowel disease type 10
- Inflammatory Bowel Disease Type 11
- Inflammatory bowel disease type 13
- Inflammatory bowel disease type 14
- Inflammatory bowel disease type 17
- Inflammatory bowel disease type 19
- Inflammatory bowel disease type 25, autosomal recessive
- Inflammatory bowel disease type 28, autosomal recessive
- Inflammatory Breast Cancer
- Inflammatory Breast Cancer in Men
- Inflammatory Breast Carcinoma
- Inflammatory conditions
- Inflammatory disorders
- Inflammatory Hepatocellular Adenoma
- Inflammatory Infiltrate
- Inflammatory Leiomyosarcoma
- Inflammatory linear verrucous epidermal nevus
- Inflammatory Liposarcoma
- Inflammatory Malignant Fibrous Histiocytoma
- Inflammatory myofibroblastic tumor
- Inflammatory myopathies
- Inflammatory Pseudotumor Intracranial
- Inflammatory skin and bowel disease, neonatal type 1
- Inflammatory skin and bowel disease, neonatal, type 2
- Influenza A H3N2
- Influenza A virus
- Influenza B Virus
- Influenza virus pneumonia
- Infratentorial cancer
- Infratentorial Glioblastoma
- Infratentorial Neoplasm
- Infrequent Neoplasm
- Infundibular Stenosis
- Infundibular-Like Structures Present
- Infundibulocystic Basal Cell Carcinoma
- Infundibulopelvic dysgenesis
- Infusion Site Extravasation
- Infusion-Related Reaction
- Ingrown hairs
- Ingrown nails
- Ingrown toenail
- Inguinal hernia
- Inguinal Lymph Node Metastasis
- Inhalant Drug Abuse
- Inhalant Drug Intoxication
- Inhalant Drug Withdrawal
- Inhalation injury
- Inhalational anthrax
- Inherited blood coagulation disease
- Inherited blood disorders
- Inherited bone marrow failure syndromes
- Inherited Color Blindness
- Inherited eye disorder
- Inherited Hemolytic Anemias
- Inherited ichthyosis
- Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
- Inherited language disorder
- Inherited Long QT Syndrome
- Inherited lung disorders
- Inherited metabolic diseases
- Inherited neurological disorders
- Inherited Neuropathies
- Inherited peripheral neuropathy
- Inherited thyroxine-binding globulin deficiency
- Iniencephaly
- Injection anthrax
- Injection Site Arthritis
- Injection Site Pain
- Injuries
- Injury in Children
- Inner Ear Disorders
- Inner Ear Infection
- Inner Ear Neoplasm
- Innocent Heart Murmurs
- Inosine triphosphatase deficiency
- Insect Allergies
- Insect bites
- Insect stings
- ...and more....
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Note: This site is for informational purposes only and is not medical advice. See your doctor or other qualified medical professional for all your medical needs.