| OMIM ID |
Human Disease |
| 242150 |
Ichthyosiform Erythroderma, Corneal Involvement, and Deafness |
| 308200 |
Ichthyosis and Male Hypogonadism (1 mouse model) |
| 146800 |
Ichthyosis, Bullous Type (2 mouse models) |
| 146720 |
Ichthyosis--Cheek--Eyebrow Syndrome |
| 615024 |
Ichthyosis, Congenital, Autosomal Recessive 10; ARCI10 |
| 242300 |
Ichthyosis, Congenital, Autosomal Recessive 1; ARCI1 (1 mouse model) |
| 242100 |
Ichthyosis, Congenital, Autosomal Recessive 2; ARCI2 (1 mouse model) |
| 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 |
| 602400 |
Ichthyosis, Follicular Atrophoderma, Hypotrichosis, and Hypohidrosis |
| 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 |
| 614457 |
Ichthyosis, Spastic Quadriplegia, and Mental Retardation; ISQMR |
| 242550 |
Ichthyosis, Split Hairs, and Amino Aciduria |
| 146700 |
Ichthyosis Vulgaris (1 mouse model) |
| 242510 |
Ichthyosis with Alopecia, Eclabium, Ectropion, and Mental Retardation |
| 610765 |
Ichthyosis with Hypotrichosis, Autosomal Recessive |
| 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 |
| 208155 |
Illum Syndrome |
| 601174 |
Imidazoline Receptor |
| 242600 |
Iminoglycinuria |
| 242700 |
Immune Defect Due to Absence of Thymus |
| 242850 |
Immune Deficiency Disease |
| 146830 |
Immune Deficiency, Familial Variable |
| 612782 |
Immune Dysfunction with T-Cell Inactivation Due to Calcium Entry Defect 1 |
| 612783 |
Immune Dysfunction with T-Cell Inactivation Due to Calcium Entry Defect 2 |
| 146820 |
Immune Response to Synthetic Polypeptide--Irgat; IGAT |
| 146810 |
Immune Response to Synthetic Polypeptide--Irphegal; IPHEG |
| 146850 |
Immune Suppression; IS |
| 242860 |
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1; ICF1 (7 mouse models) |
| 614069 |
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2; ICF2 |
| 607594 |
Immunodeficiency, Common Variable, 1; CVID1 (2 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 |
| 610163 |
Immunodeficiency Due to Defect in Cd3-Zeta |
| 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 model) |
| 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 and Frontotemporal Dementia; IBMPFD (3 mouse models) |
| 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 |
| 269920 |
Infantile Sialic Acid Storage Disorder (1 mouse model) |
| 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 (4 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 model) |
| 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 |
| 601489 |
Insulin-Like Growth Factor-Binding Protein, Acid-Labile Subunit; IGFALS (3 mouse models) |
| 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 |
| 603783 |
Intelligence Quantitative Trait Locus 1 |
| 610294 |
Intelligence Quantitative Trait Locus 2 |
| 610295 |
Intelligence Quantitative Trait Locus 3 |
| 147560 |
Interferon Antiviral Depressor |
| 606367 |
Interleukin 2 Receptor, Alpha, Deficiency of |
| 614752 |
Interleukin 6, Serum Level of, Quantitative Trait Locus |
| 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 model) |
| 603932 |
Intervertebral Disc Disease; IDD |
| 243150 |
Intestinal Atresia, Multiple (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 |
| 611522 |
Intraocular Pressure Quantitative Trait Locus; IOPQTL |
| 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 model) |
| 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 |
Analysis Tools