List of diseases (I)
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Diseases |
Ib
Ic
Icf
Ich
- Ichthyophobia
- Ichthyosiform erythroderma corneal involvement deafness
- Ichthyosis alopecia eclabion ectropion mental retardation
- Ichthyosis and male hypogonadism
- Ichthyosis bullosa of Siemens
- Ichthyosis cheek eyebrow syndrome
- Ichthyosis congenita biliary atresia
- Ichthyosis deafness mental retardation skeletal anomaly
- Ichthyosis follicularis atrichia photophobia syndrome
- Ichthyosis hepatosplenomegaly cerebellar degeneration
- Ichthyosis hystrix, Curth Macklin type
- Ichthyosis linearis circumflexa
- Ichthyosis male hypogonadism
- Ichthyosis mental retardation Devriendt type
- Ichthyosis mental retardation dwarfism renal impairment
- Ichthyosis microphthalmos
- Ichthyosis tapered fingers midline groove up
- Ichthyosis vulgaris
- Ichthyosis, erythrokeratolysis hemalis
- Ichthyosis, keratosis follicularis spinulosa Decalvans
- Ichthyosis, lamellar recessive
- Ichthyosis, Netherton syndrome
Id
- Idaho syndrome
- Idiopathic acute eosinophilic pneumonia
- Idiopathic adolescent scoliosis
- Idiopathic adult neutropenia
- Idiopathic alveolar hypoventilation syndrome
- Idiopathic congenital nystagmus, dominant, X- linked
- Idiopathic diffuse interstitial fibrosis
- Idiopathic dilatation of the pulmonary artery
- Idiopathic dilation cardiomyopathy
- Idiopathic double athetosis
- Idiopathic edema
- Idiopathic eosinophilic chronic pneumopathy
- Idiopathic facial palsy
- Idiopathic hypereosinophilic syndrome
- Idiopathic infection caused by BCG or atypical mycobacteria
- Idiopathic juvenile osteoporosis
- Idiopathic pulmonary fibrosis
- Idiopathic pulmonary haemosiderosis
- Idiopathic sclerosing mesenteritis
- Idiopathic thrombocytopenic purpura
- Iduronate 2-sulfatase deficiency
Ie-Im
- IFAP syndrome
- IgA deficiency
- IGDA syndrome
- Illum syndrome
- Illyngophobia
- Ilyina Amoashy Grygory syndrome
- Imaizumi Kuroki syndrome
- Iminoglycinuria
- Immotile cilia syndrome, due to defective radial spokes
- Immotile cilia syndrome, due to excessively long cilia
- Immotile cilia syndrome, Kartagener type
- Immune deficiency, familial variable
- Immune thrombocytopenia
- Immunodeficiency, primary
- Immunodeficiency, secondary
- Immunodeficiency with short limb dwarfism
- Immunodeficiency, microcephaly with normal intelligence
- Imperforate anus
- Imperforate oropharynx costo vetebral anomalies
- Impossible syndrome
In
Ina
Inb-Ind
- Inborn amino acid metabolism disorder
- Inborn branched chain aminoaciduria
- Inborn error of metabolism
- Inborn metabolic disorder
- Inborn renal aminoaciduria
- Inborn urea cycle disorder
- Incisors fused
- Inclusion conjunctivitis
- Incontinentia pigmenti type 1
- Incontinentia pigmenti type 2
- Incontinentia pigmenti
- Indomethacin antenatal infection
Inf
- Infant epilepsy with migrant focal crisis
- Infant respiratory distress syndrome
- Infantile apnea
- Infantile axonal neuropathy
- Infantile convulsions and paroxysmal choreoathetosis, familial
- Infantile digital fibromatosis
- Infantile dysphagia
- Infantile multisystem inflammatory disease
- Infantile myofibromatosis
- Infantile onset spinocerebellar ataxia
- Infantile recurrent chronic multifocal osteomyolitis
- Infantile sialic acid storage disorder
- Infantile spasms broad thumbs
- Infantile spasms
- Infantile spinal muscular atrophy
- Infantile striato thalamic degeneration
- Infectious arthritis
- Infectious myocarditis
- Infective endocarditis
- Inflammatory breast cancer
- Infundibulopelvic stenosis multicystic kidney
- Influenza
- Inguinal hernia
Ins
- Congenital insensitivity to pain
- Instability mitotic non disjunction syndrome
- Insulinoma
- Insulin-resistance type B
- Insulin-resistant acanthosis nigricans, type A
Int
- Intercellular cholesterol esterification disease
- Interferon gamma, receptor 1, deficiency
- Internal carotid agenesis
- Intraocular lymphoma
- Interstitial cystitis
- Interstitial lung disease
- Interstitial pneumonia
- Intestinal atresia multiple
- Intestinal lipodystrophy
- Intestinal lymphangiectasia
- Intestinal malrotation facial anomalies familial type
- Intestinal pseudoobstruction chronic idiopathic
- Intestinal pseudo-obstruction
- Intoeing
- Intracranial aneurysms multiple congenital anomaly
- Intracranial arterioveinous malformation
- Intractable singultus
- Intrathoracic kidney vertebral fusion
- Intrauterine growth retardation mandibular malar hypoplasia
- Intrauterine infections
- Intrinsic factor, congenital deficiency of
Io-Iv
- Iodine antenatal infection
- Iodine deficiency
- Iophobia
- Iridocyclitis
- Iridogoniodysgenesis, dominant type
- Iris dysplasia hypertelorism deafness
- Iritis
- Irons Bhan syndrome
- Irritable bowel syndrome
- Isaacs Mertens syndrome
- Isaacs syndrome
- Ischiadic hypoplasia renal dysfunction immunodeficiency
- Ischiopatellar dysplasia
- Isosporosiasis
- Isotretinoin embryopathy
- Isthmian coarctation
- Ivemark syndrome
- Ivic Syndrome
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
