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Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

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Human Diseases/Syndromes Beginning with "I"

To see all annotations for a disease, click the disease name.

OMIM IDHuman Disease
OMIM:242150 Ichthyosiform Erythroderma, Corneal Involvement, and Deafness
OMIM:308200 Ichthyosis and Male Hypogonadism
OMIM:146800 Ichthyosis Bullosa of Siemens; IBS
OMIM:146720 Ichthyosis--Cheek--Eyebrow Syndrome
OMIM:615024 Ichthyosis, Congenital, Autosomal Recessive 10; ARCI10
OMIM:602400 Ichthyosis, Congenital, Autosomal Recessive 11; ARCI11
OMIM:617320 Ichthyosis, Congenital, Autosomal Recessive 12; ARCI12
OMIM:242300 Ichthyosis, Congenital, Autosomal Recessive 1; ARCI1
OMIM:242100 Ichthyosis, Congenital, Autosomal Recessive 2; ARCI2
OMIM:606545 Ichthyosis, Congenital, Autosomal Recessive 3; ARCI3
OMIM:601277 Ichthyosis, Congenital, Autosomal Recessive 4A; ARCI4A
OMIM:242500 Ichthyosis, Congenital, Autosomal Recessive 4b; ARCI4B
OMIM:604777 Ichthyosis, Congenital, Autosomal Recessive 5; ARCI5
OMIM:612281 Ichthyosis, Congenital, Autosomal Recessive 6; ARCI6
OMIM:615022 Ichthyosis, Congenital, Autosomal Recessive 7; ARCI7
OMIM:613943 Ichthyosis, Congenital, Autosomal Recessive 8; ARCI8
OMIM:615023 Ichthyosis, Congenital, Autosomal Recessive 9; ARCI9
OMIM:242400 Ichthyosis Congenita with Biliary Atresia
OMIM:607602 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis
OMIM:242520 Ichthyosis, Hepatosplenomegaly, and Cerebellar Degeneration
OMIM:146590 Ichthyosis Hystrix, Curth-Macklin Type; IHCM
OMIM:146600 Ichthyosis Hystrix Gravior
OMIM:602540 Ichthyosis, Hystrix-Like, with Deafness
OMIM:146750 Ichthyosis, Lamellar, Autosomal Dominant
OMIM:607626 Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis;
OMIM:242530 Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment
OMIM:601039 Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin
OMIM:608649 Ichthyosis Prematurity Syndrome; IPS
OMIM:614457 Ichthyosis, Spastic Quadriplegia, and Mental Retardation; ISQMR
OMIM:242550 Ichthyosis, Split Hairs, and Amino Aciduria
OMIM:146700 Ichthyosis Vulgaris
OMIM:242510 Ichthyosis with Alopecia, Eclabium, Ectropion, and Mental Retardation
OMIM:300001 Ichthyosis, X-Linked, without Steroid Sulfatase Deficiency
OMIM:308100 Ichthyosis, X-Linked; XLI
OMIM:308205 Ifap Syndrome with or without Bresheck Syndrome
OMIM:161950 Iga Nephropathy, Susceptibility to, 1; IGAN1
OMIM:613944 Iga Nephropathy, Susceptibility to, 2; IGAN2
OMIM:616818 Iga Nephropathy, Susceptibility to, 3; IGAN3
OMIM:147050 IgE Responsiveness, Atopic; IGER
OMIM:615207 Il21r Immunodeficiency
OMIM:208155 Illum Syndrome
OMIM:242600 Iminoglycinuria
OMIM:242700 Immune Defect Due to Absence of Thymus
OMIM:242850 Immune Deficiency Disease
OMIM:146830 Immune Deficiency, Familial Variable
OMIM:146850 Immune Suppression; IS
OMIM:612783 Immunodeficiency 10; IMD10
OMIM:615206 Immunodeficiency 11; IMD11
OMIM:615468 Immunodeficiency 12; IMD12
OMIM:615518 Immunodeficiency 13; IMD13
OMIM:615513 Immunodeficiency 14; IMD14
OMIM:615592 Immunodeficiency 15; IMD15
OMIM:615593 Immunodeficiency 16; IMD16
OMIM:615607 Immunodeficiency 17; IMD17
OMIM:615615 Immunodeficiency 18; IMD18
OMIM:615617 Immunodeficiency 19; IMD19
OMIM:615707 Immunodeficiency 20; IMD20
OMIM:614172 Immunodeficiency 21; IMD21
OMIM:615758 Immunodeficiency 22; IMD22
OMIM:615816 Immunodeficiency 23; IMD23
OMIM:615897 Immunodeficiency 24; IMD24
OMIM:610163 Immunodeficiency 25; IMD25
OMIM:615966 Immunodeficiency 26 with or without Neurologic Abnormalities; IMD26
OMIM:209950 Immunodeficiency 27a; IMD27A
OMIM:615978 Immunodeficiency 27b; IMD27B
OMIM:614889 Immunodeficiency 28; IMD28
OMIM:614890 Immunodeficiency 29; IMD29
OMIM:614891 Immunodeficiency 30; IMD30
OMIM:614892 Immunodeficiency 31a; IMD31A
OMIM:613796 Immunodeficiency 31b; IMD31B
OMIM:614162 Immunodeficiency 31c; IMD31C
OMIM:614893 Immunodeficiency 32a; IMD32A
OMIM:614894 Immunodeficiency 32b; IMD32B
OMIM:300636 Immunodeficiency 33; IMD33
OMIM:300645 Immunodeficiency 34; IMD34
OMIM:611521 Immunodeficiency 35; IMD35
OMIM:616005 Immunodeficiency 36; IMD36
OMIM:616098 Immunodeficiency 37; IMD37
OMIM:616126 Immunodeficiency 38 with Basal Ganglia Calcification; IMD38
OMIM:616345 Immunodeficiency 39; IMD39
OMIM:616433 Immunodeficiency 40; IMD40
OMIM:606367 Immunodeficiency 41 with Lymphoproliferation and Autoimmunity; IMD41
OMIM:616622 Immunodeficiency 42; IMD42
OMIM:241600 Immunodeficiency 43; IMD43
OMIM:616636 Immunodeficiency 44; IMD44
OMIM:616669 Immunodeficiency 45; IMD45
OMIM:616740 Immunodeficiency 46; IMD46
OMIM:300972 Immunodeficiency 47; IMD47
OMIM:269840 Immunodeficiency 48; IMD48
OMIM:617237 Immunodeficiency 49; IMD49
OMIM:300988 Immunodeficiency 50; IMD50
OMIM:613953 Immunodeficiency 51; IMD51
OMIM:617514 Immunodeficiency 52; IMD52
OMIM:615401 Immunodeficiency 8; IMD8
OMIM:612782 Immunodeficiency 9; IMD9
OMIM:242860 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1; ICF1
OMIM:614069 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2; ICF2
OMIM:616910 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 3; ICF3
OMIM:616911 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 4; ICF4
OMIM:615577 Immunodeficiency, Common Variable, 10; CVID10
OMIM:615767 Immunodeficiency, Common Variable, 11; CVID11
OMIM:616576 Immunodeficiency, Common Variable, 12; CVID12
OMIM:616873 Immunodeficiency, Common Variable, 13; CVID13
OMIM:607594 Immunodeficiency, Common Variable, 1; CVID1
OMIM:240500 Immunodeficiency, Common Variable, 2; CVID2
OMIM:613493 Immunodeficiency, Common Variable, 3; CVID3
OMIM:613494 Immunodeficiency, Common Variable, 4; CVID4
OMIM:613495 Immunodeficiency, Common Variable, 5; CVID5
OMIM:613496 Immunodeficiency, Common Variable, 6; CVID6
OMIM:614699 Immunodeficiency, Common Variable, 7; CVID7
OMIM:614700 Immunodeficiency, Common Variable, 8, with Autoimmunity; CVID8
OMIM:610798 Immunodeficiency Due to Defect in Mapbp-Interacting Protein
OMIM:611926 Immunodeficiency, Ovarian Dysgenesis, and Pulmonary Fibrosis
OMIM:242870 Immunodeficiency, Partial Combined, with Absence of HLA Determinants and Beta-2-Microglobulin From Lymphocytes
OMIM:146840 Immunodeficiency with Defective Leukocyte and Lymphocyte Function and with Response to Histamine-1 Antagonist
OMIM:243110 Immunodeficiency with Defective T-Cell Response to Interleukin 1
OMIM:308230 Immunodeficiency with Hyper-IgM, Type 1; HIGM1
OMIM:605258 Immunodeficiency with Hyper-Igm, Type 2; HIGM2
OMIM:606843 Immunodeficiency with Hyper-Igm, Type 3; HIGM3
OMIM:608184 Immunodeficiency with Hyper-Igm, Type 4; HIGM4
OMIM:608106 Immunodeficiency with Hyper-Igm, Type 5; HIGM5
OMIM:300584 Immunodeficiency without Anhidrotic Ectodermal Dysplasia
OMIM:308220 Immunodeficiency, X-Linked, with Deficiency of 115,000 Dalton Surface Glycoprotein
OMIM:300853 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia; XMEN
OMIM:304790 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked;
OMIM:242880 Immunoerythromyeloid Hypoplasia
OMIM:137100 Immunoglobulin A Deficiency 1; IGAD1
OMIM:609529 Immunoglobulin A Deficiency 2; IGAD2
OMIM:242890 Immunoglobulin D Level in Plasma, Low
OMIM:614102 Immunoglobulin Kappa Light Chain Deficiency; IGKCD
OMIM:308250 Immunoglobulin M, Level of
OMIM:147260 Immunoglobulin Switch Sequences
OMIM:300076 Immunoneurologic Disorder, X-Linked
OMIM:617425 Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities; ISDNA
OMIM:308280 Impacted Teeth, Multiple
OMIM:308290 Imprinting Gene Related to Retinoblastoma
OMIM:147251 Incisors, Fused Mandibular
OMIM:147300 Incisors, Long Upper Central
OMIM:147330 Incisors, Lower Central, Absence of
OMIM:147350 Incisors, Rotation of Upper Central
OMIM:147400 Incisors, Shovel-Shaped
OMIM:167320 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1; IBMPFD1
OMIM:615422 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 2; IBMPFD2
OMIM:615424 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 3; IBMPFD3
OMIM:147421 Inclusion Body Myositis
OMIM:308300 Incontinentia Pigmenti; IP
OMIM:147430 Indifference to Pain, Congenital, Autosomal Dominant
OMIM:243000 Indifference to Pain, Congenital, Autosomal Recessive; CIP
OMIM:243050 Indolylacroyl Glycinuria with Mental Retardation
OMIM:614559 Infantile Cerebellar-Retinal Degeneration; ICRD
OMIM:615438 Infantile Liver Failure Syndrome 1; ILFS1
OMIM:616483 Infantile Liver Failure Syndrome 2; ILFS2
OMIM:269920 Infantile Sialic Acid Storage Disease; ISSD
OMIM:613759 Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations
OMIM:191390 Inflammatory Bowel Disease 11; IBD11
OMIM:612241 Inflammatory Bowel Disease 12; IBD12
OMIM:612244 Inflammatory Bowel Disease 13; IBD13
OMIM:612245 Inflammatory Bowel Disease 14; IBD14
OMIM:612255 Inflammatory Bowel Disease 15; IBD15
OMIM:612259 Inflammatory Bowel Disease 16; IBD16
OMIM:612261 Inflammatory Bowel Disease 17; IBD17
OMIM:612262 Inflammatory Bowel Disease 18; IBD18
OMIM:612288 Inflammatory Bowel Disease 20; IBD20
OMIM:612354 Inflammatory Bowel Disease 21; IBD21
OMIM:612380 Inflammatory Bowel Disease 22; IBD22
OMIM:612381 Inflammatory Bowel Disease 23; IBD23
OMIM:612566 Inflammatory Bowel Disease 24; IBD24
OMIM:612567 Inflammatory Bowel Disease 25, Autosomal Recessive; IBD25
OMIM:612639 Inflammatory Bowel Disease 26; IBD26
OMIM:612796 Inflammatory Bowel Disease 27; IBD27
OMIM:613148 Inflammatory Bowel Disease 28, Autosomal Recessive; IBD28
OMIM:601458 Inflammatory Bowel Disease 2; IBD2
OMIM:604519 Inflammatory Bowel Disease 3; IBD3
OMIM:606675 Inflammatory Bowel Disease 4; IBD4
OMIM:606348 Inflammatory Bowel Disease 5; IBD5
OMIM:606674 Inflammatory Bowel Disease 6; IBD6
OMIM:605225 Inflammatory Bowel Disease 7; IBD7
OMIM:606668 Inflammatory Bowel Disease 8; IBD8
OMIM:608448 Inflammatory Bowel Disease 9; IBD9
OMIM:611081 Inflammatory Bowel Disease (crohn Disease) 10; IBD10
OMIM:612278 Inflammatory Bowel Disease (crohn Disease) 19; IBD19
OMIM:266600 Inflammatory Bowel Disease (crohn Disease) 1; IBD1
OMIM:614328 Inflammatory Skin and Bowel Disease, Neonatal, 1; NISBD1
OMIM:616069 Inflammatory Skin and Bowel Disease, Neonatal, 2; NISBD2
OMIM:614680 Influenza, Severe, Susceptibility to
OMIM:600989 Infundibulopelvic Dysgenesis
OMIM:243080 Inosine Phosphorylase Deficiency, Immune Defect Due to
OMIM:613850 Inosine Triphosphatase Deficiency
OMIM:147540 Insect Stings, Hypersensitivity to
OMIM:256800 Insensitivity to Pain, Congenital, with Anhidrosis; CIPA
OMIM:147530 Insensitivity to Pain with Hyperplastic Myelinopathy
OMIM:608747 Insulin-Like Growth Factor I Deficiency
OMIM:270450 Insulin-Like Growth Factor I, Resistance to
OMIM:606960 Insulinoma Tumor Suppressor Gene Locus
OMIM:147320 Insulin Receptors, Familial Increase in
OMIM:147545 Insulin Receptor Substrate 1; IRS1
OMIM:173470 Integrin, Beta-3; ITGB3
OMIM:617173 Intellectual Developmental Disorder with Cardiac Arrhythmia; IDDCA
OMIM:617333 Intellectual Developmental Disorder with Dysmorphic Facies and Ptosis; IDDDFP
OMIM:617452 Intellectual Developmental Disorder with Dysmorphic Facies, Seizures, and Distal Limb Anomalies; IDDFSDA
OMIM:617450 Intellectual Developmental Disorder with Gastrointestinal Difficulties and High Pain Threshold; IDDGIP
OMIM:617532 Intellectual Developmental Disorder with Neuropsychiatric Features;
OMIM:617101 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin
OMIM:147560 Interferon Antiviral Depressor
OMIM:243100 Internal Carotid Arteries, Hypoplasia of
OMIM:147820 Internal Carotid Artery, Spontaneous Dissection of
OMIM:615486 Interstitial Lung and Liver Disease; ILLD
OMIM:614748 Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital; ILNEB
OMIM:614817 Interstitial Nephritis, Karyomegalic; KMIN
OMIM:263000 Interstitial Pneumonitis, Desquamative, Familial; DIP
OMIM:603932 Intervertebral Disc Disease; IDD
OMIM:300048 Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked
OMIM:243185 Intestinal Pseudoobstruction with Patent Ductus Arteriosus and Natal Teeth
OMIM:243200 Intracranial Hypertension, Idiopathic
OMIM:614732 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies
OMIM:600546 Intrauterine Growth Retardation with Increased Mitomycin C Sensitivity
OMIM:243320 Intrinsic Factor and R Binder, Combined Congenital Deficiency of
OMIM:261000 Intrinsic Factor Deficiency; IFD
OMIM:147710 Intussusception
OMIM:610799 Invasive Pneumococcal Disease, Recurrent Isolated, 1; IPD1
OMIM:300640 Invasive Pneumococcal Disease, Recurrent Isolated, 2; IPD2
OMIM:607676 IRAK4 Deficiency
OMIM:609515 Iridogoniodysgenesis and Skeletal Anomalies
OMIM:308500 Iris Hypoplasia with Glaucoma; IHG
OMIM:610744 Iris Pattern
OMIM:601616 Iris Pigment Epithelium Anomalies
OMIM:147610 Iris Pigment Layer, Cleavage of
OMIM:601195 Iron Overload in Africa
OMIM:206200 Iron-Refractory Iron Deficiency Anemia; IRIDA
OMIM:147891 Ischiocoxopodopatellar Syndrome; ICPPS
OMIM:147630 Islet Cell Adenomatosis
OMIM:611283 Isobutyryl-Coa Dehydrogenase Deficiency
OMIM:262400 Isolated Growth Hormone Deficiency, Type IA; IGHD1A
OMIM:612781 Isolated Growth Hormone Deficiency, Type IB; IGHD1B
OMIM:173100 Isolated Growth Hormone Deficiency, Type II; IGHD2
OMIM:307200 Isolated Growth Hormone Deficiency, Type III; IGHD3
OMIM:600801 Isoproterenol-Mediated Vasodilatation
OMIM:243440 Isotretinoin Embryopathy-Like Syndrome
OMIM:243500 Isovaleric Acidemia; IVA
OMIM:243450 Isovaleric Acid, Inability to Smell
OMIM:147750 IVIC Syndrome

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last database update
07/11/2017
MGI 6.10
The Jackson Laboratory