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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"

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OMIM IDHuman Disease
OMIM:308200 Ichthyosis and Male Hypogonadism
OMIM:607602 Ichthyosis, Annular Epidermolytic, 1; AEI1
OMIM:620148 Ichthyosis, Annular Epidermolytic, 2; AEI2
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:617574 Ichthyosis, Congenital, Autosomal Recessive 13; ARCI13
OMIM:617571 Ichthyosis, Congenital, Autosomal Recessive 14; ARCI14
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:242520 Ichthyosis, Hepatosplenomegaly, and Cerebellar Degeneration
OMIM:146590 Ichthyosis Hystrix, Curth-Macklin Type; IHCM
OMIM:146600 Ichthyosis Hystrix, Lambert Type; IHL
OMIM:602540 Ichthyosis, Hystrix-Like, with Deafness
OMIM:146750 Ichthyosis, Lamellar, Autosomal Dominant; ADLI
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 Impaired Intellectual Development; ISQMR
OMIM:242550 Ichthyosis, Split Hairs, and Amino Aciduria
OMIM:146700 Ichthyosis Vulgaris
OMIM:242510 Ichthyosis with Alopecia, Eclabium, Ectropion, and Mental Retardation
OMIM:609165 Ichthyosis with Confetti; IWC
OMIM:620507 Ichthyosis with Erythrokeratoderma; IEKD
OMIM:300001 Ichthyosis, X-Linked, without Steroid Sulfatase Deficiency
OMIM:308100 Ichthyosis, X-Linked; XLI
OMIM:618527 Ichthyotic Keratoderma, Spasticity, Hypomyelination, and Dysmorphic Facial Features; IKSHD
OMIM:308205 Ifap Syndrome 1, with or without Bresheck Syndrome; IFAP1
OMIM:619016 Ifap Syndrome 2; IFAP2
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:208155 Illum Syndrome
OMIM:618786 Imagawa-Matsumoto Syndrome; IMMAS
OMIM:261100 Imerslund-Grasbeck Syndrome 1; IGS1
OMIM:618882 Imerslund-Grasbeck Syndrome 2; IGS2
OMIM:242600 Iminoglycinuria
OMIM:242850 Immune Deficiency Disease
OMIM:146830 Immune Deficiency, Familial Variable
OMIM:618998 Immune Dysregulation and Systemic Hyperinflammation Syndrome; IMDYSHI
OMIM:620514 Immune Dysregulation, Autoimmunity, and Autoinflammation; IDAA
OMIM:616100 Immune Dysregulation with Autoimmunity, Immunodeficiency, and Lymphoproliferation; IDAIL
OMIM:146850 Immune Suppression; IS
OMIM:188030 Immune Thrombocytopenia; ITP
OMIM:618042 Immunodeficiency 100 with Pulmonary Alveolar Proteinosis and Hypogammaglobulinemia; IMD100
OMIM:619872 Immunodeficiency 101 (varicella Zoster Virus-Specific); IMD101
OMIM:301082 Immunodeficiency 102; IMD102
OMIM:212050 Immunodeficiency 103, Susceptibility to Fungal Infections; IMD103
OMIM:608971 Immunodeficiency 104; IMD104
OMIM:619924 Immunodeficiency 105; IMD105
OMIM:619935 Immunodeficiency 106, Susceptibility to Viral Infections; IMD106
OMIM:619986 Immunodeficiency 107, Susceptibility to Invasive Staphylococcus Aureus Infection; IMD107
OMIM:260570 Immunodeficiency 108 with Autoinflammation; IMD108
OMIM:620282 Immunodeficiency 109 with Lymphoproliferation; IMD109
OMIM:612783 Immunodeficiency 10; IMD10
OMIM:614868 Immunodeficiency 110 with Lymphoproliferation; IMD110
OMIM:620449 Immunodeficiency 112; IMD112
OMIM:620565 Immunodeficiency 113 with Autoimmunity and Autoinflammation; IMD113
OMIM:620603 Immunodeficiency 114, Folate-Responsive; IMD114
OMIM:620632 Immunodeficiency 115 with Autoinflammation; IMD115
OMIM:608957 Immunodeficiency 116; IMD116
OMIM:620668 Immunodeficiency 117; IMD117
OMIM:301115 Immunodeficiency 118; IMD118
OMIM:615206 Immunodeficiency 11a; IMD11A
OMIM:617638 Immunodeficiency 11b with Atopic Dermatitis; IMD11B
OMIM:615468 Immunodeficiency 12; IMD12
OMIM:615518 Immunodeficiency 13; IMD13
OMIM:615513 Immunodeficiency 14a with Lymphoproliferation, Autosomal Dominant;
OMIM:619281 Immunodeficiency 14b, Autosomal Recessive; IMD14B
OMIM:618204 Immunodeficiency 15a; IMD15A
OMIM:615592 Immunodeficiency 15b; IMD15B
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:226990 Immunodeficiency 32b; IMD32B
OMIM:300636 Immunodeficiency 33; IMD33
OMIM:300645 Immunodeficiency 34; IMD34
OMIM:611521 Immunodeficiency 35; IMD35
OMIM:616005 Immunodeficiency 36 with Lymphoproliferation; 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:617585 Immunodeficiency 53; IMD53
OMIM:609981 Immunodeficiency 54; IMD54
OMIM:617827 Immunodeficiency 55; IMD55
OMIM:615207 Immunodeficiency 56; IMD56
OMIM:618108 Immunodeficiency 57 with Autoinflammation; IMD57
OMIM:618131 Immunodeficiency 58; IMD58
OMIM:233600 Immunodeficiency 59 and Hypoglycemia; IMD59
OMIM:618394 Immunodeficiency 60 and Autoimmunity; IMD60
OMIM:300310 Immunodeficiency 61; IMD61
OMIM:618459 Immunodeficiency 62; IMD62
OMIM:618495 Immunodeficiency 63 with Lymphoproliferation and Autoimmunity; IMD63
OMIM:618534 Immunodeficiency 64 with Lymphoproliferation; IMD64
OMIM:618648 Immunodeficiency 65, Susceptibility to Viral Infections; IMD65
OMIM:618847 Immunodeficiency 66; IMD66
OMIM:607676 Immunodeficiency 67; IMD67
OMIM:612260 Immunodeficiency 68; IMD68
OMIM:618963 Immunodeficiency 69; IMD69
OMIM:618969 Immunodeficiency 70; IMD70
OMIM:617718 Immunodeficiency 71 with Inflammatory Disease and Congenital Thrombocytopenia; IMD71
OMIM:618982 Immunodeficiency 72 with Autoinflammation and Lymphoproliferation;
OMIM:608203 Immunodeficiency 73a with Defective Neutrophil Chemotaxis and Leukocytosis; IMD73A
OMIM:618986 Immunodeficiency 73b with Defective Neutrophil Chemotaxis and Lymphopenia; IMD73B
OMIM:618987 Immunodeficiency 73c with Defective Neutrophil Chemotaxis and Hypogammaglobulinemia; IMD73C
OMIM:301051 Immunodeficiency 74, Covid19-Related, X-Linked; IMD74
OMIM:619126 Immunodeficiency 75 with Lymphoproliferation; IMD75
OMIM:619164 Immunodeficiency 76; IMD76
OMIM:619223 Immunodeficiency 77; IMD77
OMIM:619220 Immunodeficiency 78 with Autoimmunity and Developmental Delay; IMD78
OMIM:619238 Immunodeficiency 79; IMD79
OMIM:615387 Immunodeficiency 7; IMD7
OMIM:619313 Immunodeficiency 80 with or without Congenital Cardiomyopathy; IMD80
OMIM:619374 Immunodeficiency 81; IMD81
OMIM:619381 Immunodeficiency 82 with Systemic Inflammation; IMD82
OMIM:613002 Immunodeficiency 83, Susceptibility to Viral Infections; IMD83
OMIM:619437 Immunodeficiency 84; IMD84
OMIM:619510 Immunodeficiency 85 and Autoimmunity; IMD85
OMIM:619549 Immunodeficiency 86; IMD86
OMIM:619573 Immunodeficiency 87 and Autoimmunity; IMD87
OMIM:619630 Immunodeficiency 88; IMD88
OMIM:619632 Immunodeficiency 89 and Autoimmunity; IMD89
OMIM:615401 Immunodeficiency 8 with Lymphoproliferation; IMD8
OMIM:613759 Immunodeficiency 90 with Encephalopathy, Functional Hyposplenia, and Hepatic Dysfunction; IMD90
OMIM:619644 Immunodeficiency 91 and Hyperinflammation; IMD91
OMIM:619652 Immunodeficiency 92; IMD92
OMIM:619705 Immunodeficiency 93 and Hypertrophic Cardiomyopathy; IMD93
OMIM:619750 Immunodeficiency 94 with Autoinflammation and Dysmorphic Facies;
OMIM:619773 Immunodeficiency 95; IMD95
OMIM:619774 Immunodeficiency 96; IMD96
OMIM:619802 Immunodeficiency 97 with Autoinflammation; IMD97
OMIM:301078 Immunodeficiency 98 with Autoinflammation, X-Linked; IMD98
OMIM:619846 Immunodeficiency 99 with Hypogammaglobulinemia and Autoimmune Cytopenias; IMD99
OMIM:612782 Immunodeficiency 9; IMD9
OMIM:242860 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1;
OMIM:614069 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2;
OMIM:616910 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 3;
OMIM:616911 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 4;
OMIM:615577 Immunodeficiency, Common Variable, 10; CVID10
OMIM:615767 Immunodeficiency, Common Variable, 11; CVID11
OMIM:616576 Immunodeficiency, Common Variable, 12, with Autoimmunity; CVID12
OMIM:616873 Immunodeficiency, Common Variable, 13; CVID13
OMIM:617765 Immunodeficiency, Common Variable, 14; CVID14
OMIM:620670 Immunodeficiency, Common Variable, 15; CVID15
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:617744 Immunodeficiency, Developmental Delay, and Hypohomocysteinemia;
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: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: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:616789 Impaired Intellectual Development and Distinctive Facial Features with or without Cardiac Defects; MRFACD
OMIM:613671 Impaired Intellectual Development, Anterior Maxillary Protrusion, and Strabismus; MRAMS
OMIM:606772 Impaired Intellectual Development, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies
OMIM:610156 Impaired Intellectual Development, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome; MORMS
OMIM:617995 Impdh2 Enzyme Activity, Variation In; IMPDH2V
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:619733 Inclusion Body Myopathy and Brain White Matter Abnormalities; IBMWMA
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:243000 Indifference to Pain, Congenital, Autosomal Recessive; CIP
OMIM:243050 Indolylacroyl Glycinuria with Mental Retardation
OMIM:618339 Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development; CASGID
OMIM:614559 Infantile Cerebellar-Retinal Degeneration; ICRD
OMIM:615438 Infantile Liver Failure Syndrome 1; ILFS1
OMIM:616483 Infantile Liver Failure Syndrome 2; ILFS2
OMIM:618641 Infantile Liver Failure Syndrome 3; ILFS3
OMIM:269920 Infantile Sialic Acid Storage Disease; ISSD
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:618077 Inflammatory Bowel Disease 29; IBD29
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:619079 Inflammatory Bowel Disease (crohn Disease) 30; IBD30
OMIM:618213 Inflammatory Bowel Disease, Immunodeficiency, and Encephalopathy;
OMIM:619398 Inflammatory Bowel Disease (infantile Ulcerative Colitis) 31, Autosomal Recessive; IBD31
OMIM:620199 Inflammatory Poikiloderma with Hair Abnormalities and Acral Keratoses; IPHAK
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; IGF1D
OMIM:270450 Insulin-Like Growth Factor I, Resistance To; IGF1RES
OMIM:147630 Insulinomatosis and Diabetes Mellitus; INSDM
OMIM:606960 Insulinoma Tumor Suppressor Gene Locus
OMIM:147320 Insulin Receptors, Familial Increase in
OMIM:147545 Insulin Receptor Substrate 1; IRS1
OMIM:618195 Intellectual Developmental Disorder and Retinitis Pigmentosa; IDDRP
OMIM:614256 Intellectual Developmental Disorder, Autosomal Dominant 10; MRD10
OMIM:156200 Intellectual Developmental Disorder, Autosomal Dominant 1; MRD1
OMIM:615502 Intellectual Developmental Disorder, Autosomal Dominant 21; MRD21
OMIM:612337 Intellectual Developmental Disorder, Autosomal Dominant 22; MRD22
OMIM:615761 Intellectual Developmental Disorder, Autosomal Dominant 23; MRD23
OMIM:615834 Intellectual Developmental Disorder, Autosomal Dominant 26; MRD26
OMIM:616078 Intellectual Developmental Disorder, Autosomal Dominant 29; MRD29
OMIM:614113 Intellectual Developmental Disorder, Autosomal Dominant 2; MRD2
OMIM:616083 Intellectual Developmental Disorder, Autosomal Dominant 30, with Speech Delay and Behavioral Abnormalities; MRD30
OMIM:616311 Intellectual Developmental Disorder, Autosomal Dominant 33; MRD33
OMIM:616351 Intellectual Developmental Disorder, Autosomal Dominant 34; MRD34
OMIM:616393 Intellectual Developmental Disorder, Autosomal Dominant 38; MRD38
OMIM:616521 Intellectual Developmental Disorder, Autosomal Dominant 39; MRD39
OMIM:612580 Intellectual Developmental Disorder, Autosomal Dominant 3; MRD3
OMIM:616944 Intellectual Developmental Disorder, Autosomal Dominant 41; MRD41
OMIM:616973 Intellectual Developmental Disorder, Autosomal Dominant 42; MRD42
OMIM:616977 Intellectual Developmental Disorder, Autosomal Dominant 43; MRD43
OMIM:617061 Intellectual Developmental Disorder, Autosomal Dominant 44, with Microcephaly; MRD44
OMIM:617600 Intellectual Developmental Disorder, Autosomal Dominant 45; MRD45
OMIM:617601 Intellectual Developmental Disorder, Autosomal Dominant 46; MRD46
OMIM:617635 Intellectual Developmental Disorder, Autosomal Dominant 47; MRD47
OMIM:617751 Intellectual Developmental Disorder, Autosomal Dominant 48; MRD48
OMIM:612581 Intellectual Developmental Disorder, Autosomal Dominant 4; MRD4
OMIM:617787 Intellectual Developmental Disorder, Autosomal Dominant 50, with Behavioral Abnormalities; MRD50
OMIM:617788 Intellectual Developmental Disorder, Autosomal Dominant 51; MRD51
OMIM:617796 Intellectual Developmental Disorder, Autosomal Dominant 52; MRD52
OMIM:617798 Intellectual Developmental Disorder, Autosomal Dominant 53; MRD53
OMIM:617799 Intellectual Developmental Disorder, Autosomal Dominant 54; MRD54
OMIM:617831 Intellectual Developmental Disorder, Autosomal Dominant 55, with Seizures; MRD55
OMIM:617854 Intellectual Developmental Disorder, Autosomal Dominant 56; MRD56
OMIM:618050 Intellectual Developmental Disorder, Autosomal Dominant 57; MRD57
OMIM:618106 Intellectual Developmental Disorder, Autosomal Dominant 58; MRD58
OMIM:618522 Intellectual Developmental Disorder, Autosomal Dominant 59; MRD59
OMIM:612621 Intellectual Developmental Disorder, Autosomal Dominant 5; MRD5
OMIM:618587 Intellectual Developmental Disorder, Autosomal Dominant 60, with Seizures; MRD60
OMIM:618009 Intellectual Developmental Disorder, Autosomal Dominant 61; MRD61
OMIM:618793 Intellectual Developmental Disorder, Autosomal Dominant 62; MRD62
OMIM:618825 Intellectual Developmental Disorder, Autosomal Dominant 63, with Macrocephaly; MRD63
OMIM:619188 Intellectual Developmental Disorder, Autosomal Dominant 64; MRD64
OMIM:619320 Intellectual Developmental Disorder, Autosomal Dominant 65; MRD65
OMIM:619910 Intellectual Developmental Disorder, Autosomal Dominant 66; MRD66
OMIM:619927 Intellectual Developmental Disorder, Autosomal Dominant 67; MRD67
OMIM:619934 Intellectual Developmental Disorder, Autosomal Dominant 68; MRD68
OMIM:617863 Intellectual Developmental Disorder, Autosomal Dominant 69; MRD69
OMIM:613970 Intellectual Developmental Disorder, Autosomal Dominant 6, with or without Seizures; MRD6
OMIM:620157 Intellectual Developmental Disorder, Autosomal Dominant 70; MRD70
OMIM:620330 Intellectual Developmental Disorder, Autosomal Dominant 71, with Behavioral Abnormalities; MRD71
OMIM:620439 Intellectual Developmental Disorder, Autosomal Dominant 72; MRD72
OMIM:620450 Intellectual Developmental Disorder, Autosomal Dominant 73; MRD73
OMIM:620688 Intellectual Developmental Disorder, Autosomal Dominant 74; MRD74
OMIM:614104 Intellectual Developmental Disorder, Autosomal Dominant 7; MRD7
OMIM:611096 Intellectual Developmental Disorder, Autosomal Recessive 10; MRT10
OMIM:611097 Intellectual Developmental Disorder, Autosomal Recessive 11; MRT11
OMIM:611090 Intellectual Developmental Disorder, Autosomal Recessive 12; MRT12
OMIM:613192 Intellectual Developmental Disorder, Autosomal Recessive 13; MRT13
OMIM:614020 Intellectual Developmental Disorder, Autosomal Recessive 14; MRT14
OMIM:614208 Intellectual Developmental Disorder, Autosomal Recessive 16; MRT16
OMIM:614249 Intellectual Developmental Disorder, Autosomal Recessive 18, with or without Epilepsy; MRT18
OMIM:614343 Intellectual Developmental Disorder, Autosomal Recessive 19; MRT19
OMIM:249500 Intellectual Developmental Disorder, Autosomal Recessive 1; MRT1
OMIM:614344 Intellectual Developmental Disorder, Autosomal Recessive 23; MRT23
OMIM:614345 Intellectual Developmental Disorder, Autosomal Recessive 24; MRT24
OMIM:614346 Intellectual Developmental Disorder, Autosomal Recessive 25; MRT25
OMIM:614340 Intellectual Developmental Disorder, Autosomal Recessive 27; MRT27
OMIM:614347 Intellectual Developmental Disorder, Autosomal Recessive 28; MRT28
OMIM:614333 Intellectual Developmental Disorder, Autosomal Recessive 29; MRT29
OMIM:607417 Intellectual Developmental Disorder, Autosomal Recessive 2; MRT2
OMIM:614342 Intellectual Developmental Disorder, Autosomal Recessive 30; MRT30
OMIM:614329 Intellectual Developmental Disorder, Autosomal Recessive 31; MRT31
OMIM:614341 Intellectual Developmental Disorder, Autosomal Recessive 33; MRT33
OMIM:614499 Intellectual Developmental Disorder, Autosomal Recessive 34, with Variant Lissencephaly; MRT34
OMIM:615162 Intellectual Developmental Disorder, Autosomal Recessive 35; MRT35
OMIM:615493 Intellectual Developmental Disorder, Autosomal Recessive 37; MRT37
OMIM:615516 Intellectual Developmental Disorder, Autosomal Recessive 38; MRT38
OMIM:615541 Intellectual Developmental Disorder, Autosomal Recessive 39; MRT39
OMIM:608443 Intellectual Developmental Disorder, Autosomal Recessive 3; MRT3
OMIM:615637 Intellectual Developmental Disorder, Autosomal Recessive 41; MRT41
OMIM:615817 Intellectual Developmental Disorder, Autosomal Recessive 43; MRT43
OMIM:615942 Intellectual Developmental Disorder, Autosomal Recessive 44; MRT44
OMIM:615979 Intellectual Developmental Disorder, Autosomal Recessive 45; MRT45
OMIM:616116 Intellectual Developmental Disorder, Autosomal Recessive 46; MRT46
OMIM:616193 Intellectual Developmental Disorder, Autosomal Recessive 47; MRT47
OMIM:616269 Intellectual Developmental Disorder, Autosomal Recessive 48; MRT48
OMIM:611107 Intellectual Developmental Disorder, Autosomal Recessive 4; MRT4
OMIM:616460 Intellectual Developmental Disorder, Autosomal Recessive 50; MRT50
OMIM:616739 Intellectual Developmental Disorder, Autosomal Recessive 51; MRT51
OMIM:616887 Intellectual Developmental Disorder, Autosomal Recessive 52; MRT52
OMIM:617028 Intellectual Developmental Disorder, Autosomal Recessive 54; MRT54
OMIM:617125 Intellectual Developmental Disorder, Autosomal Recessive 56; MRT56
OMIM:617188 Intellectual Developmental Disorder, Autosomal Recessive 57; MRT57
OMIM:617270 Intellectual Developmental Disorder, Autosomal Recessive 58; MRT58
OMIM:617323 Intellectual Developmental Disorder, Autosomal Recessive 59; MRT59
OMIM:611091 Intellectual Developmental Disorder, Autosomal Recessive 5; MRT5
OMIM:617432 Intellectual Developmental Disorder, Autosomal Recessive 60; MRT60
OMIM:617773 Intellectual Developmental Disorder, Autosomal Recessive 61; MRT61
OMIM:618095 Intellectual Developmental Disorder, Autosomal Recessive 63; MRT63
OMIM:618103 Intellectual Developmental Disorder, Autosomal Recessive 64; MRT64
OMIM:618109 Intellectual Developmental Disorder, Autosomal Recessive 65; MRT65
OMIM:618221 Intellectual Developmental Disorder, Autosomal Recessive 66; MRT66
OMIM:618295 Intellectual Developmental Disorder, Autosomal Recessive 67; MRT67
OMIM:618302 Intellectual Developmental Disorder, Autosomal Recessive 68; MRT68
OMIM:618383 Intellectual Developmental Disorder, Autosomal Recessive 69; MRT69
OMIM:611092 Intellectual Developmental Disorder, Autosomal Recessive 6; MRT6
OMIM:618402 Intellectual Developmental Disorder, Autosomal Recessive 70; MRT70
OMIM:618504 Intellectual Developmental Disorder, Autosomal Recessive 71; MRT71
OMIM:618665 Intellectual Developmental Disorder, Autosomal Recessive 72; MRT72
OMIM:619717 Intellectual Developmental Disorder, Autosomal Recessive 73; MRT73
OMIM:617169 Intellectual Developmental Disorder, Autosomal Recessive 74; MRT74
OMIM:619827 Intellectual Developmental Disorder, Autosomal Recessive 75, with Neuropsychiatric Features and Variant Lissencephaly; MRT75
OMIM:619931 Intellectual Developmental Disorder, Autosomal Recessive 76; MRT76
OMIM:619988 Intellectual Developmental Disorder, Autosomal Recessive 77; MRT77
OMIM:620237 Intellectual Developmental Disorder, Autosomal Recessive 78; MRT78
OMIM:620393 Intellectual Developmental Disorder, Autosomal Recessive 79; MRT79
OMIM:611093 Intellectual Developmental Disorder, Autosomal Recessive 7; MRT7
OMIM:620653 Intellectual Developmental Disorder, Autosomal Recessive 80, with Variant Lissencephaly; MRT80
OMIM:620700 Intellectual Developmental Disorder, Autosomal Recessive 81; MRT81
OMIM:620779 Intellectual Developmental Disorder, Autosomal Recessive 82; MRT82
OMIM:611095 Intellectual Developmental Disorder, Autosomal Recessive 9; MRT9
OMIM:136630 Intellectual Developmental Disorder, Fra12a Type
OMIM:618342 Intellectual Developmental Disorder with Abnormal Behavior, Microcephaly, and Short Stature; IDDABS
OMIM:620021 Intellectual Developmental Disorder with Autism and Dysmorphic Facies; IDDADF
OMIM:615032 Intellectual Developmental Disorder with Autism and Macrocephaly;
OMIM:606053 Intellectual Developmental Disorder with Autism and Speech Delay;
OMIM:618906 Intellectual Developmental Disorder with Autistic Features and Language Delay, with or without Seizures; IDDALDS
OMIM:618725 Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or without Seizures; IDDBCS
OMIM:618316 Intellectual Developmental Disorder with Cardiac Defects and Dysmorphic Facies; IDDCDF
OMIM:618089 Intellectual Developmental Disorder with Dysmorphic Facies and Behavioral Abnormalities; IDDFBA
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:619031 Intellectual Developmental Disorder with Epilepsy, Behavioral Abnormalities, and Coarse Facies; IDDEBF
OMIM:618147 Intellectual Developmental Disorder with Hypertelorism and Distinctive Facies; IDDHDF
OMIM:618748 Intellectual Developmental Disorder with Hypotonia and Behavioral Abnormalities; IDDHBA
OMIM:619556 Intellectual Developmental Disorder with Hypotonia, Impaired Speech, and Dysmorphic Facies; IDDHISD
OMIM:618653 Intellectual Developmental Disorder with Impaired Language and Dysmorphic Facies; IDDILF
OMIM:619911 Intellectual Developmental Disorder with Language Impairment and Early-Onset Dopa-Responsive Dystonia-Parkinsonism; IDLDP
OMIM:613670 Intellectual Developmental Disorder with Language Impairment and with or without Autistic Features
OMIM:618158 Intellectual Developmental Disorder with Macrocephaly, Seizures, and Speech Delay; IDDMSSD
OMIM:300749 Intellectual Developmental Disorder with Microcephaly and Pontine and Cerebellar Hypoplasia; MICPCH
OMIM:615866 Intellectual Developmental Disorder with Microcephaly and with or without Ocular Malformations or Hypogonadotropic Hypogonadism; IDDMOH
OMIM:620007 Intellectual Developmental Disorder with Muscle Tone Abnormalities and Distal Skeletal Defects; IDDMDS
OMIM:618608 Intellectual Developmental Disorder with Nasal Speech, Dysmorphic Facies, and Variable Skeletal Anomalies; IDNADFS
OMIM:617532 Intellectual Developmental Disorder with Neuropsychiatric Features;
OMIM:620086 Intellectual Developmental Disorder with Ocular Anomalies and Distinctive Facial Features; IDDOF
OMIM:618060 Intellectual Developmental Disorder with or without Epilepsy or Cerebellar Ataxia; IDDECA
OMIM:619844 Intellectual Developmental Disorder with or without Peripheral Neuropathy; IDDPN
OMIM:619150 Intellectual Developmental Disorder with Paroxysmal Dyskinesia or Seizures; IDDPADS
OMIM:617101 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin
OMIM:618808 Intellectual Developmental Disorder with Poor Growth and with or without Seizures or Ataxia; IDPOGSA
OMIM:619000 Intellectual Developmental Disorder with Seizures and Language Delay;
OMIM:618470 Intellectual Developmental Disorder with Severe Speech and Ambulation Defects; IDDSSAD
OMIM:618687 Intellectual Developmental Disorder with Short Stature and Behavioral Abnormalities; IDDSSBA
OMIM:618453 Intellectual Developmental Disorder with Short Stature and Variable Skeletal Anomalies; IDDSSA
OMIM:606220 Intellectual Developmental Disorder with Short Stature, Facial Anomalies, and Speech Defects; IDDSFAS
OMIM:619099 Intellectual Developmental Disorder with Speech Delay and Axonal Peripheral Neuropathy; IDDSAPN
OMIM:618506 Intellectual Developmental Disorder with Speech Delay and Dysmorphic Facies; IDDSDF
OMIM:618672 Intellectual Developmental Disorder with Speech Delay, Autism, and Dysmorphic Facies; IDDSADF
OMIM:618092 Intellectual Developmental Disorder with Speech Delay, Dysmorphic Facies, and T-Cell Abnormalities; IDDSFTA
OMIM:300923 Intellectual Developmental Disorder, X-Linked 100; XLID100
OMIM:300928 Intellectual Developmental Disorder, X-Linked 101; XLID101
OMIM:300982 Intellectual Developmental Disorder, X-Linked 103; XLID103
OMIM:300983 Intellectual Developmental Disorder, X-Linked 104; XLID104
OMIM:300984 Intellectual Developmental Disorder, X-Linked 105; XLID105
OMIM:300997 Intellectual Developmental Disorder, X-Linked 106; XLID106
OMIM:301013 Intellectual Developmental Disorder, X-Linked 107; XLID107
OMIM:301024 Intellectual Developmental Disorder, X-Linked 108; MRX108
OMIM:309548 Intellectual Developmental Disorder, X-Linked 109; XLID109
OMIM:301095 Intellectual Developmental Disorder, X-Linked 110; XLID110
OMIM:301107 Intellectual Developmental Disorder, X-Linked 111; XLID111
OMIM:301111 Intellectual Developmental Disorder, X-Linked 112; XLID112
OMIM:301116 Intellectual Developmental Disorder, X-Linked 113; XLID113
OMIM:300957 Intellectual Developmental Disorder, X-Linked 12; XLID12
OMIM:300062 Intellectual Developmental Disorder, X-Linked 14; XLID14
OMIM:300844 Intellectual Developmental Disorder, X-Linked 19; XLID19
OMIM:309530 Intellectual Developmental Disorder, X-Linked 1; XLID1
OMIM:300047 Intellectual Developmental Disorder, X-Linked 20; XLID20
OMIM:300143 Intellectual Developmental Disorder, X-Linked 21; XLID21
OMIM:300046 Intellectual Developmental Disorder, X-Linked 23; XLID23
OMIM:300419 Intellectual Developmental Disorder, X-Linked 29; XLID29
OMIM:300428 Intellectual Developmental Disorder, X-Linked 2; XLID2
OMIM:300558 Intellectual Developmental Disorder, X-Linked 30; XLID30
OMIM:300849 Intellectual Developmental Disorder, X-Linked 41; XLID41
OMIM:300372 Intellectual Developmental Disorder, X-Linked 42; XLID42
OMIM:300498 Intellectual Developmental Disorder, X-Linked 45; XLID45
OMIM:300436 Intellectual Developmental Disorder, X-Linked 46; XLID46
OMIM:300115 Intellectual Developmental Disorder, X-Linked 50; XLID50
OMIM:300324 Intellectual Developmental Disorder, X-Linked 53; XLID53
OMIM:300210 Intellectual Developmental Disorder, X-Linked 58; XLID58
OMIM:300387 Intellectual Developmental Disorder, X-Linked 63; XLID63
OMIM:300271 Intellectual Developmental Disorder, X-Linked 72; XLID72
OMIM:300355 Intellectual Developmental Disorder, X-Linked 73; XLID73
OMIM:300454 Intellectual Developmental Disorder, X-Linked 77; XLID77
OMIM:300433 Intellectual Developmental Disorder, X-Linked 81; XLID81
OMIM:300518 Intellectual Developmental Disorder, X-Linked 82; XLID82
OMIM:300505 Intellectual Developmental Disorder, X-Linked 84; XLID84
OMIM:300852 Intellectual Developmental Disorder, X-Linked 88; XLID88
OMIM:300848 Intellectual Developmental Disorder, X-Linked 89; XLID89
OMIM:300850 Intellectual Developmental Disorder, X-Linked 90; XLID90
OMIM:300577 Intellectual Developmental Disorder, X-Linked 91; XLID91
OMIM:300851 Intellectual Developmental Disorder, X-Linked 92; XLID92
OMIM:300659 Intellectual Developmental Disorder, X-Linked 93; XLID93
OMIM:300716 Intellectual Developmental Disorder, X-Linked 95; XLID95
OMIM:300802 Intellectual Developmental Disorder, X-Linked 96; XLID96
OMIM:300803 Intellectual Developmental Disorder, X-Linked 97; XLID97
OMIM:300912 Intellectual Developmental Disorder, X-Linked 98; XLID98
OMIM:300968 Intellectual Developmental Disorder, X-Linked 99, Syndromic, Female-Restricted; MRXS99F
OMIM:300919 Intellectual Developmental Disorder, X-Linked 99; XLID99
OMIM:309549 Intellectual Developmental Disorder, X-Linked 9; XLID9
OMIM:309545 Intellectual Developmental Disorder, X-Linked, Syndromic 12; MRXS12
OMIM:300055 Intellectual Developmental Disorder, X-Linked, Syndromic 13; MRXS13
OMIM:300676 Intellectual Developmental Disorder, X-Linked, Syndromic 14; MRXS14
OMIM:300858 Intellectual Developmental Disorder, X-Linked, Syndromic 17; MRXS17
OMIM:300886 Intellectual Developmental Disorder, X-Linked, Syndromic 32; MRXS32
OMIM:300966 Intellectual Developmental Disorder, X-Linked, Syndromic 33; MRXS33
OMIM:300967 Intellectual Developmental Disorder, X-Linked, Syndromic 34; MRXS34
OMIM:300998 Intellectual Developmental Disorder, X-Linked, Syndromic 35; MRXS35
OMIM:301118 Intellectual Developmental Disorder, X-Linked, Syndromic 37; MRXS37
OMIM:300218 Intellectual Developmental Disorder, X-Linked, Syndromic 7; MRXS7
OMIM:300709 Intellectual Developmental Disorder, X-Linked, Syndromic 9; MRXS9
OMIM:300262 Intellectual Developmental Disorder, X-Linked, Syndromic, Abidi Type;
OMIM:300261 Intellectual Developmental Disorder, X-Linked, Syndromic, Armfield Type; MRXSA
OMIM:300986 Intellectual Developmental Disorder, X-Linked, Syndromic, Bain Type;
OMIM:300486 Intellectual Developmental Disorder, X-Linked, Syndromic, Billuart Type; MRXSBL
OMIM:300354 Intellectual Developmental Disorder, X-Linked, Syndromic, Cabezas Type; MRXSC
OMIM:300243 Intellectual Developmental Disorder, X-Linked, Syndromic, Christianson Type; MRXSCH
OMIM:300861 Intellectual Developmental Disorder, X-Linked, Syndromic, Chudley-Schwartz Type; MRXSCS
OMIM:300534 Intellectual Developmental Disorder, X-Linked, Syndromic, Claes-Jensen Type; MRXSCJ
OMIM:309555 Intellectual Developmental Disorder, X-Linked, Syndromic, Gustavson Type; MRXSG
OMIM:301039 Intellectual Developmental Disorder, X-Linked, Syndromic, Hackmann-Di Donato Type; MRXSHD
OMIM:300423 Intellectual Developmental Disorder, X-Linked, Syndromic, Hedera Type; MRXSH
OMIM:301008 Intellectual Developmental Disorder, X-Linked, Syndromic, Houge Type;
OMIM:300260 Intellectual Developmental Disorder, X-Linked, Syndromic, Lubs Type;
OMIM:309520 Intellectual Developmental Disorder, X-Linked, Syndromic, Lujan-Fryns Type; MRXSLF
OMIM:300860 Intellectual Developmental Disorder, X-Linked, Syndromic, Nascimento Type; MRXSN
OMIM:301076 Intellectual Developmental Disorder, X-Linked, Syndromic, Pilorge Type; MRXSP
OMIM:300799 Intellectual Developmental Disorder, X-Linked, Syndromic, Raymond Type; MRXSR
OMIM:300238 Intellectual Developmental Disorder, X-Linked, Syndromic, Shashi Type; MRXSSH
OMIM:300263 Intellectual Developmental Disorder, X-Linked, Syndromic, Siderius Type; MRXSSD
OMIM:300958 Intellectual Developmental Disorder, X-Linked, Syndromic, Snijders Blok Type; MRXSSB
OMIM:309583 Intellectual Developmental Disorder, X-Linked, Syndromic, Snyder-Robinson Type; MRXSSR
OMIM:300434 Intellectual Developmental Disorder, X-Linked, Syndromic, Stocco Dos Santos Type; SDSX
OMIM:309590 Intellectual Developmental Disorder, X-Linked, Syndromic, Turner Type; MRXST
OMIM:309585 Intellectual Developmental Disorder, X-Linked, Syndromic, Wilson-Turner Type; WTS
OMIM:301066 Intellectual Developmental Disorder, X-Linked, Syndromic, with Pigmentary Mosaicism and Coarse Facies; MRXSPF
OMIM:300699 Intellectual Developmental Disorder, X-Linked, Syndromic, Wu Type;
OMIM:300123 Intellectual Developmental Disorder, X-Linked, with Panhypopituitarism
OMIM:619719 Intellectual Disability and Myopathy Syndrome; IDMYS
OMIM:309580 Intellectual Disability-Hypotonic Facies Syndrome, X-Linked, 1;
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:619611 Interstitial Lung Disease 1; ILD1
OMIM:178500 Interstitial Lung Disease 2; ILD2
OMIM:614817 Interstitial Nephritis, Karyomegalic; KMIN
OMIM:263000 Interstitial Pneumonitis, Desquamative, Familial; DIP
OMIM:603932 Intervertebral Disc Disease; IDD
OMIM:620045 Intestinal Dysmotility Syndrome; IDMTS
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; IMAGE
OMIM:618336 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, Genital Anomalies, and Immunodeficiency; IMAGEI
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: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:620121 Iron Overload, Susceptibility To; IO
OMIM:206200 Iron-Refractory Iron Deficiency Anemia; IRIDA
OMIM:147891 Ischiocoxopodopatellar Syndrome with or without Pulmonary Arterial Hypertension; ICPPS
OMIM:611283 Isobutyryl-Coa Dehydrogenase Deficiency; IBDD
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, with Agammaglobulinemia; IGHD3
OMIM:618157 Isolated Growth Hormone Deficiency, Type IV; IGHD4
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; IVIC
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04/30/2024
MGI 6.23 		The Jackson Laboratory