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Rare conditions starting with I
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256 conditions starting with I
- Ichthyosis
- Ichthyosis bullosa of Siemens
- Ichthyosis hystrix of Curth-Macklin
- Ichthyosis linearis circumflexa
- Ichthyosis prematurity syndrome
- Ichthyosis vulgaris
- Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome
- Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome
- Ichthyosis-oral and digital anomalies syndrome
- Ichthyosis, cerebellar degeneration and hepatosplenomegaly
- Idiopathic achalasia
- Idiopathic acute eosinophilic pneumonia
- Idiopathic bronchiectasis
- Idiopathic camptocormia
- Idiopathic CD4 lymphocytopenia
- Idiopathic chronic eosinophilic pneumonia
- Idiopathic congenital hypothyroidism
- Idiopathic disseminated cytomegalovirus infection
- Idiopathic hypersomnia
- Idiopathic inflammatory myopathy
- Idiopathic juvenile osteoporosis
- Idiopathic malabsorption due to bile acid synthesis defects
- Idiopathic membranous glomerulonephritis
- Idiopathic pulmonary artery dilatation
- Idiopathic Pulmonary Fibrosis
- Idiopathic pulmonary hemosiderosis
- Idiopathic spontaneous coronary artery dissection
- IFAP syndrome
- IgA glomerulonephritis
- IgG4-related dacryoadenitis and sialadenitis
- IgG4-related mediastinitis
- IgG4-related pachymeningitis
- IgG4-related retroperitoneal fibrosis
- Iida Kannari syndrome
- IL10-related early-onset inflammatory bowel disease
- IL21-related infantile inflammatory bowel disease
- IMAGe syndrome
- Imerslund-Grasbeck syndrome
- Iminoglycinuria
- Immotile cilia syndrome due to defective radial spokes
- Immotile cilia syndrome due to excessively long cilia
- Immune deficiency, familial variable
- Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome
- Immunodeficiency 23
- Immunodeficiency 32B
- Immunodeficiency 33
- Immunodeficiency 61
- Immunodeficiency 67
- Immunodeficiency 79
- Immunodeficiency due to a classical component pathway complement deficiency
- Immunodeficiency due to a late component of complement deficiency
- Immunodeficiency due to CD25 deficiency
- Immunodeficiency due to ficolin3 deficiency
- Immunodeficiency due to MASP-2 deficiency
- Immunodeficiency with factor H anomaly
- Immunodeficiency with thymoma
- Immunoglobulin A deficiency 2
- Immunoglobulin A vasculitis
- Immunoglobulin G4-related sclerosing disease
- Immunotactoid glomerulopathy
- Immunotactoid or fibrillary glomerulopathy
- Imperforate anus
- Imperforate oropharynx-costo vertebral anomalies syndrome
- Inborn carbohydrate metabolic disorder
- Inborn organic aciduria
- Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
- Inclusion body myositis
- Incontinentia pigmenti syndrome
- Infant epilepsy with migrant focal crisis
- Infantile apnea
- Infantile bilateral striatal necrosis
- Infantile cerebellar-retinal degeneration
- Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- Infantile choroidocerebral calcification syndrome
- Infantile convulsions and choreoathetosis
- Infantile cortical hyperostosis
- Infantile digital fibromatosis
- Infantile epileptic dyskinetic encephalopathy
- Infantile GM1 gangliosidosis
- Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
- Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
- Infantile Krabbe disease
- Infantile liver failure
- Infantile liver failure syndrome 1
- Infantile liver failure syndrome 2
- Infantile myofibromatosis
- Infantile neuroaxonal dystrophy
- Infantile neuronal ceroid lipofuscinosis
- Infantile onset spinocerebellar ataxia
- Infantile osteopetrosis with neuroaxonal dysplasia
- Infantile spasms-broad thumbs syndrome
- Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome
- Infantile-onset ascending hereditary spastic paralysis
- Infantile-onset autosomal recessive nonprogressive cerebellar ataxia
- Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome
- Infantile-onset generalized dyskinesia with orofacial involvement
- Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
- Infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia
- Infantile-onset X-linked spinal muscular atrophy
- Infection by Dracunculus medinensis
- Infection by larvae of Trichinella
- Infection by Paragonimus
- Infection by Strongyloides
- Infection by Trypanosoma cruzi
- Infection due to clostridium perfringens
- Infection due to Mycobacterium xenopi
- Infectious myositis
- Infective dermatitis associated with HTLV-1
- Infective endocarditis
- Infertility associated with multi-tailed spermatozoa and excessive DNA
- Inflammatory bowel disease-recurrent sinopulmonary infections syndrome
- Inflammatory bowel disease, immunodeficiency, and encephalopathy
- Inflammatory breast carcinoma
- Inflammatory linear verrucous epidermal nevus
- Inflammatory myofibroblastic tumor
- Infundibulopelvic stenosis-multicystic kidney syndrome
- Inhalational anthrax
- Inherited acute myeloid leukemia
- Inherited Creutzfeldt-Jakob disease
- Inherited glutathione synthetase deficiency
- Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
- Inherited lipoic acid biosynthesis defect
- Inherited porphyria
- Inherited prekallikrein deficiency
- Inherited pseudoxanthoma elasticum
- Inherited susceptibility to mycobacterial diseases
- Iniencephaly
- Insulin autoimmune syndrome
- Insulin-dependent diabetes mellitus secretory diarrhea syndrome
- Insulin-resistance syndrome type B
- Insulin-resistant diabetes mellitus AND acanthosis nigricans
- Intellectual developmental disorder with cardiac defects and dysmorphic facies
- Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
- Intellectual developmental disorder with seizures and language delay
- Intellectual disability-balding-patella luxation-acromicria syndrome
- Intellectual disability-brachydactyly-Pierre Robin syndrome
- Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome
- Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome
- Intellectual disability-epilepsy-extrapyramidal syndrome
- Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
- Intellectual disability-facial dysmorphism-hand anomalies syndrome
- Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
- Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome
- Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome
- Intellectual disability-hypotonia-spasticity-sleep disorder syndrome
- Intellectual disability-hypotonic facies syndrome, X-linked, 1
- Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome
- Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome
- Intellectual disability-myopathy-short stature-endocrine defect syndrome
- Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome
- Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome
- Intellectual disability-polydactyly-uncombable hair syndrome
- Intellectual disability-seizures-macrocephaly-obesity syndrome
- Intellectual disability-severe speech delay-mild dysmorphism syndrome
- Intellectual disability-short stature-hypertelorism syndrome
- Intellectual disability-spasticity-ectrodactyly syndrome
- Intellectual disability-strabismus syndrome
- Intellectual disability, anterior maxillary protrusion, and strabismus
- Intellectual disability, autosomal dominant 29
- Intellectual disability, autosomal dominant 30
- Intellectual disability, autosomal dominant 40
- Intellectual disability, autosomal dominant 42
- Intellectual disability, autosomal dominant 43
- Intellectual disability, autosomal dominant 47
- Intellectual disability, autosomal dominant 48
- Intellectual disability, autosomal dominant 5
- Intellectual disability, autosomal dominant 6
- Intellectual disability, autosomal recessive 58
- Intellectual disability, Buenos-Aires type
- Intellectual disability, Wolff type
- Intellectual disability, X-linked 1
- Intellectual disability, X-linked 49
- Intellectual disability, X-linked 63
- Intellectual disability, X-linked syndromic, Turner type
- Intellectual disability, X-linked, syndromic 33
- Intellectual disability, X-linked, syndromic, Bain type
- Intellectual disability, X-linked, with or without seizures, ARX-related
- Intermediate DEND syndrome
- Intermediate nemaline myopathy
- Intermittent hydrarthrosis
- Internal carotid agenesis
- Interstitial cystitis
- Interstitial lung disease due to ABCA3 deficiency
- Intestinal hypomagnesemia 1
- Intestinal lymphangiectasia
- Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency
- Intestinal pseudo-obstruction
- Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked
- Intracranial berry aneurysm
- Intractable diarrhea-choanal atresia-eye anomalies syndrome
- Intradural spinal arachnoid cyst
- Intrahepatic cholangiocarcinoma
- Intraneural perineurioma
- Intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome
- Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome
- Intrauterine growth retardation with increased mitomycin c sensitivity
- Invasive non-typhoidal salmonellosis
- Irido-corneo-trabecular dysgenesis
- Iridocorneal endothelial syndrome
- Iris coloboma
- Iris hypoplasia with glaucoma
- Iron-refractory iron deficiency anemia
- IRVAN syndrome
- Isaac syndrome
- Ischio-vertebral syndrome
- Isochromosomy Yp
- Isochromosomy Yq
- Isolated agammaglobulinemia
- Isolated anhidrosis with normal sweat glands
- Isolated aniridia
- Isolated ankyloblepharon filiforme adnatum
- Isolated anophthalmia-microphthalmia syndrome
- Isolated anterior cervical hypertrichosis
- Isolated asymptomatic elevation of creatine phosphokinase
- Isolated autosomal dominant hypomagnesemia, Glaudemans type
- Isolated cleft palate
- Isolated congenital alacrima
- Isolated congenital breast hypoplasia/aplasia
- Isolated congenital digital clubbing
- Isolated congenital ectropion
- Isolated congenital growth hormone deficiency
- Isolated congenital hypoglossia/aglossia
- Isolated congenital hypogonadotropic hypogonadism
- Isolated congenital megalocornea
- Isolated congenital microcephaly
- Isolated congenital syngnathia
- Isolated cryptophthalmia
- Isolated delta-storage pool disease
- Isolated ectopia lentis
- Isolated encephalocele
- Isolated focal cortical dysplasia
- Isolated focal cortical dysplasia type II
- Isolated glycerol kinase deficiency
- Isolated growth hormone deficiency type IB
- Isolated hemihyperplasia
- Isolated hereditary congenital facial paralysis
- Isolated hyperchlorhidrosis
- Isolated lissencephaly type 1 without known genetic defect
- Isolated lutropin deficiency
- Isolated microcephaly
- Isolated microphthalmia 5
- Isolated neonatal sclerosing cholangitis
- Isolated optic nerve hypoplasia
- Isolated osteopoikilosis
- Isolated Pierre-Robin syndrome
- Isolated right ventricular hypoplasia
- Isolated sedoheptulokinase deficiency
- Isolated spina bifida
- Isolated thyroid-stimulating hormone deficiency
- Isolated tracheo-esophageal fistula
- Isosporiasis
- Isotretinoin-like syndrome
- Isovaleryl-CoA dehydrogenase deficiency
- ITM2B amyloidosis
- Ito hypomelanosis
- ITP
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