Disease Search
- Illum syndrome
- Imerslund-Grasbeck syndrome
- Iminoglycinuria
- Immotile Cilia Syndrome
- Immune defect due to absence of thymus
- Immune Deficiency Disorder
- Immune deficiency function with T-cell inactivation due to calcium entry defect 1
- Immune deficiency function with T-cell inactivation due to calcium entry defect 2
- Immune deficiency, familial variable
- Immune dysfunction with T-cell inactivation due to calcium entry defect 1
- Immune dysfunction with T-cell inactivation due to calcium entry defect 2
- Immune thrombocytopenia
- Immune Thrombocytopenic Purpura
- Immunodeficiency 33, mycobacteriosis
- Immunodeficiency 43
- Immunodeficiency due to defect in cd3-zeta
- Immunodeficiency due to defect in mapbp-interacting protein
- Immunodeficiency due to ficolin 3 deficiency
- 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 without anhidrotic ectodermal dysplasia
- Immunodeficiency, common variable, 1
- Immunodeficiency, common variable, 3
- Immunodeficiency, common variable, 4
- Immunodeficiency, common variable, 5
- Immunodeficiency, common variable, 6
- Immunodeficiency, microcephaly with normal intelligence
- Immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection, and neoplasia
- Immunodeficiency-centromeric instability-facial anomalies syndrome 2
- Immunodysregulation, polyendocrinopathy and enteropathy X-linked
- Immunoglobulin A deficiency 2
- Immunoglobulin E, Basic Level of, in Serum
- Immunoglobulin G deficiency
- Immunoglobulin kappa light chain deficiency
- Impairment of oral perception
- Imperforate anus
- Imperforate oropharynx costo vetebral anomalies
- Impetigo
- Inborn amino acid metabolism disorder
- Inborn branched chain aminoaciduria
- Inborn Errors of Metabolism
- Inborn renal aminoaciduria
- Inclusion body myopathy 2
- Inclusion body myopathy 3
- Inclusion body myopathy with early-onset paget disease and frontotemporal dementia
- Inclusion Body Myositis
- Inclusion conjunctivitis
- Incontinence
- Incontinentia pigmenti
- Increased analgesia from kappa-opioid receptor agonist, female-specific
- Indian blood group system
- Indifference to pain, congenital, autosomal recessive
- Indigestion
- Indolent B cell lymphoma
- Infant epilepsy with migrant focal crisis
- Infantile agranulocytosis
- Infantile apnea
- Infantile axonal neuropathy
- Infantile bilateral striatal necrosis
- Infantile carnitine palmitoyltransferase II deficiency
- Infantile cerebellar-retinal degeneration
- Infantile convulsions and paroxysmal choreoathetosis, familial
- Infantile cortical hyperostosis
- Infantile digital fibromatosis
- Infantile dysphagia
- Infantile epileptic encephalopathy 13 (EIEE13)
- Infantile GM1 gangliosidosis
- Infantile histiocytoid cardiomyopathy
- Infantile hypercalcemia
- Infantile hypophosphatasia
- Infantile multisystem inflammatory disease
- Infantile myofibromatosis
- Infantile nephronophthisis
- Infantile Neuroaxonal Dystrophy (INAD)
- Infantile onset spinocerebellar ataxia
- Infantile Parkinsonism-dystonia
- Infantile recurrent chronic multifocal osteomyolitis
- Infantile Refsum's disease
- Infantile sialic acid storage disorder
- Infantile spasms
- Infantile spasms broad thumbs
- Infantile striato thalamic degeneration
- Infantile striatonigral degeneration
- Infantile Systemic Hyalinosis
- Infantile-onset ascending hereditary spastic paralysis
- Infection by Trichuris trichiura
- Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations
- Infectious arthritis
- Infectious myocarditis
- Infective endocarditis
- Infective myositis
- Infertility
- Infertility associated with multi-tailed spermatozoa and excessive DNA
- Inflammatory bowel disease
- Inflammatory breast cancer
- Inflammatory linear verrucous epidermal nevus
- Inflammatory myofibroblastic tumor
- Inflammatory myofibroblastic tumor of the breast
- Inflammatory Myopathies
- Inflammatory skin and bowel disease, neonatal
- Influenza
- Infundibulopelvic dysgenesis
- Ingrown hair
- Ingrown toenail
- Inherited hypoprothrombinemia
- Inherited peripheral neuropathy
- Inherited Thrombocytopenia
- Iniencephaly
- Inosine triphosphatase deficiency
- Insensitivity to pain, congenital, with anhidrosis
- Insomnia
- Insulin-dependent diabetes mellitus secretory diarrhea syndrome
- Insulin-like growth factor 1 resistance to
- Insulin-like growth factor I deficiency
- Insulin-resistance type B
- Insulin-resistant acanthosis nigricans, type A
- Insulin-resistant diabetes mellitus AND acanthosis nigricans
- Insulinoma
- Intellectual deficit Buenos-Aires type
- Intellectual developmental disorder
- Intellectual disability
- Intellectual disability with language impairment and autistic features
- Intercellular cholesterol esterification disease
- Interferon gamma, receptor 1, deficiency
- Interleukin 2 receptor, alpha, deficiency of
- Interleukin-1 Receptor Antagonist Defiency
- Internal carotid agenesis
- Intersex conditions
- Interstitial cystitis
- Interstitial Duplication 15q
- Interstitial Lung Disease
- Interventricular communication
- Intervertebral disc disease
- Intervertebral disc disorder
- Intestinal atresia multiple
- Intestinal enterokinase deficiency
- Intestinal Multiple Polyposis
- Intestinal pseudo-obstruction
- Intestinal Pseudo-Obstruction Syndrome
- Intestinal pseudoobstruction neuronal chronic idiopathic X-linked
- Intestinal pseudoobstruction with external ophthalmoplegia
- Intracranial aneurysms multiple congenital anomaly
- Intracranial arteriovenous malformation
- Intracranial Hypertension
- Intractable hiccups
- Intrahepatic bile duct cancer
- Intrahepatic cholangiocarcinoma
- Intraocular melanoma
- Intraoperative floppy iris syndrome (IFIS)
- Intrathoracic kidney vertebral fusion
- Intrauterine Growth Restriction (IUGR)
- Intrauterine growth retardation with increased mitomycin C sensitivity
- Intravascular papillary endothelial hyperplasia
- Intravenous leiomyomatosis
- Intraventricular Conduct Defect
- Intrinsic factor deficiency
- Intrinsic factor, congenital deficiency of
- Intussusception
- Invasive candidiasis
- Invasive ductal carcinoma
- Invasive ductal carcinoma, breast cancer
- Invasive lobular carcinoma
- Invasive lobular carcinoma, breast cancer
- Invasive pneumococcal disease, recurrent isolated, 1
- Invasive pneumococcal disease, recurrent isolated, 2
- Invasive Strep A infection
- Iodine accumulation, transport or trapping effect
- Iodotyrosine deiodination defect
- Iodotyrosyl coupling defect
- Ion Channelopathies