Rare Diseases and Related Terms
Rare diseases terms are either (1) terms for which information requests have
been made to the Office of Rare Diseases Research, the Genetic and Rare Diseases
Information Center, or the National Human Genome Research Institute; or (2)
diseases that have been suggested as being rare. The purpose of the Rare
Diseases and Related Terms list is to distribute information; although the list
is updated regularly, it should not be used as a reference or guarantee that a
condition is rare. The prevalence of a rare disease is usually an estimate and
may change over time. A rare (or orphan) disease is generally considered to have
a prevalence of fewer than 200,000 affected individuals in the United States.
Certain diseases with 200,000 or more affected individuals may be included in
this list if certain subpopulations of people who have the disease are equal to
the prevalence standard for rare diseases. We welcome suggestions for additions
to or deletions from the list. Your recommendations may be sent via e-mail to
ord@od.nih.gov
Browse by Condition
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I cell disease
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IBIDS syndrome
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ICF syndrome
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Ichthyosiform erythroderma, corneal involvement, deafness
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Ichthyosiform erythroderma, nonbullous congenital
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Ichthyosis alopecia eclabion ectropion mental retardation
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Ichthyosis and male hypogonadism
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Ichthyosis bullosa of Siemens
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Ichthyosis cheek eyebrow syndrome
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Ichthyosis congenita biliary atresia
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Ichthyosis congenita, Harlequin fetus type
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Ichthyosis deafness mental retardation skeletal anomaly
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Ichthyosis follicularis atrichia photophobia syndrome
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Ichthyosis hepatosplenomegaly cerebellar degeneration
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Ichthyosis hystrix gravior
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Ichthyosis hystrix, Curth Macklin type
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Ichthyosis lamellar 1
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Ichthyosis lamellar 2
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Ichthyosis lamellar 3
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Ichthyosis lamellar, autosomal dominant
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Ichthyosis lamellar, recessive
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Ichthyosis linearis circumflexa
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Ichthyosis male hypogonadism
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Ichthyosis mental retardation dwarfism renal impairment
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Ichthyosis microphthalmos
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Ichthyosis prematurity syndrome
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Ichthyosis tapered fingers midline groove up
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Ichthyosis vulgaris
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Ichthyosis with hypotrichosis, autosomal recessive
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Ichthyosis, acquired
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Ichthyosis, erythrokeratolysis hemalis
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Ichthyosis, follicular
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Ichthyosis, keratosis follicularis spinulosa decalvans
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Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
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Ichthyosis, mental retardation, dwarfism and renal impairment
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Ichthyosis-mental retardation syndrome with large keratohyalin granules in the skin
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Idiopathic acute eosinophilic pneumonia
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Idiopathic adolescent scoliosis
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Idiopathic alveolar hypoventilation syndrome
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Idiopathic atypical mycobacterial infection
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Idiopathic basal ganglia calcification 1
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Idiopathic basal ganglia calcification 2
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Idiopathic diffuse interstitial fibrosis
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Idiopathic dilatation of the pulmonary artery
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Idiopathic dilated cardiomyopathy
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Idiopathic double athetosis
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Idiopathic eosinophilic chronic pneumopathy
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Idiopathic hypereosinophilic syndrome
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Idiopathic minimal change nephrotic syndrome
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Idiopathic myopathy
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Idiopathic pulmonary fibrosis
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Idiopathic pulmonary hemosiderosis
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Idiopathic pulmonary hypertension
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Idiopathic subglottic tracheal stenosis
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Iida Kannari syndrome
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Illum syndrome
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Ilyina Amoashy Grygory syndrome
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Imaizumi Kuroki syndrome
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Iminoglycinuria
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Immotile cilia syndrome, due to defective radial spokes
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Immotile cilia syndrome, due to excessively long cilia
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Immune defect due to absence of thymus
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Immune deficiency function with T-cell inactivation due to calcium entry defect 1
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Immune deficiency function with T-cell inactivation due to calcium entry defect 2
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Immune deficiency, familial variable
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Immune thrombocytopenia
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Immunodeficiency with hyper IgM type 1
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Immunodeficiency with hyper IgM type 2
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Immunodeficiency with hyper IgM type 3
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Immunodeficiency with hyper IgM type 4
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Immunodeficiency with hyper IgM type 5
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Immunodeficiency without anhidrotic ectodermal dysplasia
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Immunodeficiency, microcephaly with normal intelligence
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Immunodysregulation, polyendocrinopathy and enteropathy X-linked
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Immunoglobulin A deficiency 2
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Impairment of oral perception
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Imperforate anus
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Imperforate oropharynx costo vetebral anomalies
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Impossible syndrome
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Inborn amino acid metabolism disorder
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Inborn branched chain aminoaciduria
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Inborn renal aminoaciduria
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Incisors fused
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Inclusion body myopathy 2
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Inclusion body myopathy 3
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Inclusion conjunctivitis
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Incontinentia pigmenti
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Indolent B cell lymphoma
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Indomethacin antenatal infection
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Infant epilepsy with migrant focal crisis
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Infantile apnea
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Infantile axonal neuropathy
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Infantile convulsions and paroxysmal choreoathetosis, familial
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Infantile digital fibromatosis
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Infantile dysphagia
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Infantile histiocytoid cardiomyopathy
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Infantile multisystem inflammatory disease
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Infantile myofibromatosis
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Infantile onset spinocerebellar ataxia
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Infantile Parkinsonism-dystonia and elevated dopamine metabolites in CSF
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Infantile recurrent chronic multifocal osteomyolitis
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Infantile sialic acid storage disorder
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Infantile spasms
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Infantile spasms broad thumbs
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Infantile striato thalamic degeneration
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Infantile-onset ascending hereditary spastic paralysis
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Infectious arthritis
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Infectious myocarditis
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Infective endocarditis
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Infective myositis
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Inflammatory breast cancer
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Inflammatory myofibroblastic tumor of the breast
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Infundibulopelvic dysgenesis
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Inherited hypoprothrombinemia
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Iniencephaly
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Insensitivity to pain, congenital, with anhidrosis
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Insulin-like growth factor 1 resistance to
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Insulin-like growth factor I deficiency
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Insulinoma
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Insulin-resistance type B
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Insulin-resistant acanthosis nigricans, type A
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Intercellular cholesterol esterification disease
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Interferon gamma, receptor 1, deficiency
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Internal carotid agenesis
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Intervertebral disc disease
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Intestinal atresia multiple
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Intestinal malrotation facial anomalies familial type
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Intestinal pseudo-obstruction
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Intestinal pseudoobstruction chronic idiopathic
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Intracranial aneurysms multiple congenital anomaly
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Intracranial arteriovenous malformation
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Intrahepatic cholangiocarcinoma
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Intraocular melanoma
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Intrathoracic kidney vertebral fusion
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Intrauterine growth retardation mandibular malar hypoplasia
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Intrauterine growth retardation with increased mitomycin C sensitivity
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Intrauterine infections
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Intrinsic factor, congenital deficiency of
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Iodine antenatal infection
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IRAK4 deficiency
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Iridogoniodysgenesis and skeletal anomalies
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Iridogoniodysgenesis type1
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Iridogoniodysgenesis, dominant type
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Iris dysplasia hypertelorism deafness
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Iris hypoplasia and glaucoma
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Irons Bhan syndrome
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Isaacs syndrome
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Ischiadic hypoplasia renal dysfunction immunodeficiency
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Ischiopatellar dysplasia
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Isobutyryl-CoA dehydrogenase deficiency
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Isolated growth hormone deficiency type 1A
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Isolated growth hormone deficiency type 1B
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Isolated growth hormone deficiency type 2
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Isolated growth hormone deficiency type 3
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Isosporosiasis
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Isotretinoin embryopathy like syndrome
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Isthmian coarctation
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Ivemark syndrome
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IVIC syndrome