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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
242150 Ichthyosiform Erythroderma, Corneal Involvement, and Deafness
308200 Ichthyosis and Male Hypogonadism (1 mouse models)
146800 Ichthyosis, Bullous Type (2 mouse models)
146720 Ichthyosis--Cheek--Eyebrow Syndrome
615024 Ichthyosis, Congenital, Autosomal Recessive 10; ARCI10
602400 Ichthyosis, Congenital, Autosomal Recessive 11; ARCI11
242300 Ichthyosis, Congenital, Autosomal Recessive 1; ARCI1 (1 mouse models)
242100 Ichthyosis, Congenital, Autosomal Recessive 2; ARCI2 (1 mouse models)
606545 Ichthyosis, Congenital, Autosomal Recessive 3; ARCI3
601277 Ichthyosis, Congenital, Autosomal Recessive 4A; ARCI4A
242500 Ichthyosis, Congenital, Autosomal Recessive 4b; ARCI4B (5 mouse models)
604777 Ichthyosis, Congenital, Autosomal Recessive 5; ARCI5
612281 Ichthyosis, Congenital, Autosomal Recessive 6; ARCI6
615022 Ichthyosis, Congenital, Autosomal Recessive 7; ARCI7
613943 Ichthyosis, Congenital, Autosomal Recessive 8; ARCI8
615023 Ichthyosis, Congenital, Autosomal Recessive 9; ARCI9
242400 Ichthyosis Congenita with Biliary Atresia
607602 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis
242520 Ichthyosis, Hepatosplenomegaly, and Cerebellar Degeneration
146590 Ichthyosis Hystrix, Curth-Macklin Type; IHCM
146600 Ichthyosis Hystrix Gravior
602540 Ichthyosis, Hystrix-Like, with Deafness
146750 Ichthyosis, Lamellar, Autosomal Dominant
607626 Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis
242530 Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment
601039 Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin
608649 Ichthyosis Prematurity Syndrome; IPS (1 mouse models)
614457 Ichthyosis, Spastic Quadriplegia, and Mental Retardation; ISQMR
242550 Ichthyosis, Split Hairs, and Amino Aciduria
146700 Ichthyosis Vulgaris (1 mouse models)
242510 Ichthyosis with Alopecia, Eclabium, Ectropion, and Mental Retardation
300001 Ichthyosis, X-Linked, without Steroid Sulfatase Deficiency
308100 Ichthyosis, X-Linked; XLI
308205 Ifap Syndrome with or without Bresheck Syndrome
161950 Iga Nephropathy, Susceptibility to, 1; IGAN1 (2 mouse models)
613944 Iga Nephropathy, Susceptibility to, 2; IGAN2
147050 IgE Responsiveness, Atopic; IGER
615207 Il21r Immunodeficiency
208155 Illum Syndrome
242600 Iminoglycinuria
242700 Immune Defect Due to Absence of Thymus
242850 Immune Deficiency Disease
146830 Immune Deficiency, Familial Variable
146850 Immune Suppression; IS
612783 Immunodeficiency 10; IMD10
615206 Immunodeficiency 11; IMD11
615468 Immunodeficiency 12; IMD12
615518 Immunodeficiency 13; IMD13
615513 Immunodeficiency 14; IMD14
615592 Immunodeficiency 15; IMD15
615593 Immunodeficiency 16; IMD16
615607 Immunodeficiency 17; IMD17
615615 Immunodeficiency 18; IMD18
615617 Immunodeficiency 19; IMD19
615707 Immunodeficiency 20; IMD20
614172 Immunodeficiency 21; IMD21
615758 Immunodeficiency 22; IMD22
615816 Immunodeficiency 23; IMD23
615897 Immunodeficiency 24; IMD24
610163 Immunodeficiency 25; IMD25
615966 Immunodeficiency 26 with or without Neurologic Abnormalities; IMD26
209950 Immunodeficiency 27a; IMD27A
615978 Immunodeficiency 27b; IMD27B
614889 Immunodeficiency 28; IMD28
614890 Immunodeficiency 29; IMD29
614891 Immunodeficiency 30; IMD30
614892 Immunodeficiency 31a; IMD31A
613796 Immunodeficiency 31b; IMD31B
614893 Immunodeficiency 32a; IMD32A
300636 Immunodeficiency 33; IMD33
300645 Immunodeficiency 34; IMD34
611521 Immunodeficiency 35; IMD35
616005 Immunodeficiency 36; IMD36
615401 Immunodeficiency 8; IMD8
612782 Immunodeficiency 9; IMD9
242860 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1; ICF1 (7 mouse models)
614069 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2; ICF2
615577 Immunodeficiency, Common Variable, 10; CVID10
615767 Immunodeficiency, Common Variable, 11; CVID11
607594 Immunodeficiency, Common Variable, 1; CVID1 (5 mouse models)
240500 Immunodeficiency, Common Variable, 2; CVID2
613493 Immunodeficiency, Common Variable, 3; CVID3
613494 Immunodeficiency, Common Variable, 4; CVID4
613495 Immunodeficiency, Common Variable, 5; CVID5
613496 Immunodeficiency, Common Variable, 6; CVID6
614699 Immunodeficiency, Common Variable, 7; CVID7
614700 Immunodeficiency, Common Variable, 8, with Autoimmunity; CVID8
615559 Immunodeficiency, Common Variable, 9; CVID9
610798 Immunodeficiency Due to Defect in Mapbp-Interacting Protein
613860 Immunodeficiency Due to Ficolin 3 Deficiency
611926 Immunodeficiency, Ovarian Dysgenesis, and Pulmonary Fibrosis
242870 Immunodeficiency, Partial Combined, with Absence of HLA Determinants and Beta-2-Microglobulin From Lymphocytes
146840 Immunodeficiency with Defective Leukocyte and Lymphocyte Function and with Response to Histamine-1 Antagonist
243110 Immunodeficiency with Defective T-Cell Response to Interleukin 1
308230 Immunodeficiency with Hyper-IgM, Type 1; HIGM1
605258 Immunodeficiency with Hyper-Igm, Type 2; HIGM2
606843 Immunodeficiency with Hyper-Igm, Type 3; HIGM3
608184 Immunodeficiency with Hyper-Igm, Type 4; HIGM4
608106 Immunodeficiency with Hyper-Igm, Type 5; HIGM5
300584 Immunodeficiency without Anhidrotic Ectodermal Dysplasia
308220 Immunodeficiency, X-Linked, with Deficiency of 115,000 Dalton Surface Glycoprotein
300853 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia; XMEN
304790 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked; (2 mouse models)
242880 Immunoerythromyeloid Hypoplasia
137100 Immunoglobulin A Deficiency 1; IGAD1
609529 Immunoglobulin A Deficiency 2; IGAD2
242890 Immunoglobulin D Level in Plasma, Low
614102 Immunoglobulin Kappa Light Chain Deficiency; IGKCD
308250 Immunoglobulin M, Level of
147260 Immunoglobulin Switch Sequences
300076 Immunoneurologic Disorder, X-Linked
242900 Immunoosseous Dysplasia, Schimke Type (1 mouse models)
308280 Impacted Teeth, Multiple
308290 Imprinting Gene Related to Retinoblastoma
147251 Incisors, Fused Mandibular
147300 Incisors, Long Upper Central
147330 Incisors, Lower Central, Absence of
147350 Incisors, Rotation of Upper Central
147400 Incisors, Shovel-Shaped
600737 Inclusion Body Myopathy 2, Autosomal Recessive; IBM2
605637 Inclusion Body Myopathy 3, Autosomal Dominant; IBM3
167320 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1; IBMPFD1 (5 mouse models)
615422 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 2; IBMPFD2
615424 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 3; IBMPFD3
147421 Inclusion Body Myositis (2 mouse models)
308300 Incontinentia Pigmenti; IP (2 mouse models)
147430 Indifference to Pain, Congenital, Autosomal Dominant
243000 Indifference to Pain, Congenital, Autosomal Recessive
243050 Indolylacroyl Glycinuria with Mental Retardation
614559 Infantile Cerebellar-Retinal Degeneration; ICRD
615438 Infantile Liver Failure Syndrome 1; ILFS1
615486 Infantile Liver Failure Syndrome 2; ILFS2
269920 Infantile Sialic Acid Storage Disease; ISSD (1 mouse models)
613759 Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations
611081 Inflammatory Bowel Disease 10; IBD10 (2 mouse models)
191390 Inflammatory Bowel Disease 11; IBD11
612241 Inflammatory Bowel Disease 12; IBD12 (3 mouse models)
612244 Inflammatory Bowel Disease 13; IBD13
612245 Inflammatory Bowel Disease 14; IBD14
612255 Inflammatory Bowel Disease 15; IBD15
612259 Inflammatory Bowel Disease 16; IBD16 (2 mouse models)
612261 Inflammatory Bowel Disease 17; IBD17
612262 Inflammatory Bowel Disease 18; IBD18
612278 Inflammatory Bowel Disease 19; IBD19
266600 Inflammatory Bowel Disease 1; IBD1 (1 mouse models)
612288 Inflammatory Bowel Disease 20; IBD20
612354 Inflammatory Bowel Disease 21; IBD21
612380 Inflammatory Bowel Disease 22; IBD22
612381 Inflammatory Bowel Disease 23; IBD23 (3 mouse models)
612566 Inflammatory Bowel Disease 24; IBD24
612567 Inflammatory Bowel Disease 25, Autosomal Recessive; IBD25
612639 Inflammatory Bowel Disease 26; IBD26
612796 Inflammatory Bowel Disease 27; IBD27
613148 Inflammatory Bowel Disease 28, Autosomal Recessive; IBD28
601458 Inflammatory Bowel Disease 2; IBD2
604519 Inflammatory Bowel Disease 3; IBD3
606675 Inflammatory Bowel Disease 4; IBD4
606348 Inflammatory Bowel Disease 5; IBD5
606674 Inflammatory Bowel Disease 6; IBD6
605225 Inflammatory Bowel Disease 7; IBD7
606668 Inflammatory Bowel Disease 8; IBD8
608448 Inflammatory Bowel Disease 9; IBD9
614328 Inflammatory Skin and Bowel Disease, Neonatal; NISBD
614680 Influenza, Severe, Susceptibility to
600989 Infundibulopelvic Dysgenesis
243080 Inosine Phosphorylase Deficiency, Immune Defect Due to
613850 Inosine Triphosphatase Deficiency
147540 Insect Stings, Hypersensitivity to
256800 Insensitivity to Pain, Congenital, with Anhidrosis; CIPA (2 mouse models)
147530 Insensitivity to Pain with Hyperplastic Myelinopathy
176730 Insulin; INS
608747 Insulin-Like Growth Factor I Deficiency
270450 Insulin-Like Growth Factor I, Resistance to
606960 Insulinoma Tumor Suppressor Gene Locus
147320 Insulin Receptors, Familial Increase in
147545 Insulin Receptor Substrate 1; IRS1
173470 Integrin, Beta-3; ITGB3
147560 Interferon Antiviral Depressor
606367 Interleukin 2 Receptor, Alpha, Deficiency of
243100 Internal Carotid Arteries, Hypoplasia of
147820 Internal Carotid Artery, Spontaneous Dissection of
614748 Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital
614817 Interstitial Nephritis, Karyomegalic; KMIN
263000 Interstitial Pneumonitis, Desquamative, Familial; DIP (1 mouse models)
603932 Intervertebral Disc Disease; IDD
243150 Intestinal Atresia, Multiple; MINAT (2 mouse models)
300048 Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked
243185 Intestinal Pseudoobstruction with Patent Ductus Arteriosus and Natal Teeth
243200 Intracranial Hypertension, Idiopathic
614732 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies
600546 Intrauterine Growth Retardation with Increased Mitomycin C Sensitivity
243320 Intrinsic Factor and R Binder, Combined Congenital Deficiency of
261000 Intrinsic Factor Deficiency; IFD
147710 Intussusception
610799 Invasive Pneumococcal Disease, Recurrent Isolated, 1; IPD1
300640 Invasive Pneumococcal Disease, Recurrent Isolated, 2; IPD2
607676 IRAK4 Deficiency
609515 Iridogoniodysgenesis and Skeletal Anomalies
601631 Iridogoniodysgenesis, Type 1; IRID1
137600 Iridogoniodysgenesis, Type 2; IRID2
308500 Iris Hypoplasia with Glaucoma; IHG
610744 Iris Pattern
601616 Iris Pigment Epithelium Anomalies
147610 Iris Pigment Layer, Cleavage of
601195 Iron Overload in Africa
206200 Iron-Refractory Iron Deficiency Anemia; IRIDA
147630 Islet Cell Adenomatosis
611283 Isobutyryl-Coa Dehydrogenase Deficiency
262400 Isolated Growth Hormone Deficiency, Type IA; IGHD1A (1 mouse models)
612781 Isolated Growth Hormone Deficiency, Type IB; IGHD1B
173100 Isolated Growth Hormone Deficiency, Type II; IGHD2 (2 mouse models)
307200 Isolated Growth Hormone Deficiency, Type III; IGHD3
600801 Isoproterenol-Mediated Vasodilatation
243440 Isotretinoin Embryopathy-Like Syndrome
243500 Isovaleric Acidemia; IVA
243450 Isovaleric Acid, Inability to Smell
147750 IVIC Syndrome

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last database update
10/08/2014
MGI 5.20
The Jackson Laboratory