| OMIM ID |
Human Disease |
| 247990 |
MacDermot-Winter Syndrome |
| 109150 |
Machado-Joseph Disease; MJD (11 mouse models) |
| 248000 |
Macrocephaly |
| 613075 |
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis |
| 605309 |
Macrocephaly/Autism Syndrome |
| 153470 |
Macrocephaly, Benign Familial |
| 614192 |
Macrocephaly, Macrosomia, Facial Dysmorphism Syndrome; MMFD |
| 607131 |
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies |
| 600084 |
Macrocytosis, Familial (1 mouse model) |
| 248010 |
Macroepiphyseal Dysplasia with Osteoporosis, Wrinkled Skin, and Aged Appearance |
| 153600 |
Macroglobulinemia, Waldenstrom, Susceptibility to, 1; WM1 |
| 610430 |
Macroglobulinemia, Waldenstrom, Susceptibility to, 2; WM2 |
| 153630 |
Macroglossia |
| 602499 |
Macrophthalmia, Colobomatous, with Microcornea; MACOM |
| 248100 |
Macrosomia Adiposa Congenita |
| 248110 |
Macrosomia with Microphthalmia, Lethal |
| 613545 |
Macrostomia, Isolated |
| 600208 |
Macrothrombocytopenia and Progressive Sensorineural Deafness |
| 613112 |
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related |
| 611488 |
Macular Degeneration, Age-Related, 10; ARMD10 |
| 611953 |
Macular Degeneration, Age-Related, 11; ARMD11 |
| 613784 |
Macular Degeneration, Age-Related, 12; ARMD12 (3 mouse models) |
| 603075 |
Macular Degeneration, Age-Related, 1; ARMD1 (2 mouse models) |
| 153800 |
Macular Degeneration, Age-Related, 2; ARMD2 (3 mouse models) |
| 608895 |
Macular Degeneration, Age-Related, 3; ARMD3 |
| 610698 |
Macular Degeneration, Age-Related, 4; ARMD4 |
| 613761 |
Macular Degeneration, Age-Related, 5; ARMD5 |
| 613757 |
Macular Degeneration, Age-Related, 6; ARMD6 |
| 610149 |
Macular Degeneration, Age-Related, 7; ARMD7 |
| 613778 |
Macular Degeneration, Age-Related, 8; ARMD8 |
| 611378 |
Macular Degeneration, Age-Related, 9; ARMD9 |
| 300834 |
Macular Degeneration, X-Linked Atrophic |
| 153840 |
Macular Dystrophy, Atypical Vitelliform; VMD1 |
| 608970 |
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 |
| 153870 |
Macular Dystrophy, Concentric Annular |
| 217800 |
Macular Dystrophy, Corneal, 1; MCDC1 |
| 153890 |
Macular Dystrophy, Fenestrated Sheen Type |
| 136550 |
Macular Dystrophy, Retinal, 1, North Carolina Type; MCDR1 |
| 608051 |
Macular Dystrophy, Retinal, 2; MCDR2 |
| 608850 |
Macular Dystrophy, Retinal, 3 |
| 608161 |
Macular Dystrophy, Vitelliform, Adult-Onset |
| 153700 |
Macular Dystrophy, Vitelliform; VMD (2 mouse models) |
| 309100 |
Macular Dystrophy, X-Linked |
| 153880 |
Macular Edema, Cystoid |
| 154000 |
Macules, Hereditary Congenital Hypopigmented and Hyperpigmented |
| 248260 |
Magnesium, Elevated Red Cell |
| 266920 |
Mainzer-Saldino Syndrome; MZSDS |
| 609628 |
Majeed Syndrome |
| 125480 |
Major Affective Disorder 1; MAFD1 |
| 309200 |
Major Affective Disorder 2; MAFD2 |
| 609633 |
Major Affective Disorder 3; MAFD3 |
| 611247 |
Major Affective Disorder 4; MAFD4 |
| 611535 |
Major Affective Disorder 5; MAFD5 |
| 611536 |
Major Affective Disorder 6; MAFD6 |
| 612371 |
Major Affective Disorder 7; MAFD7 |
| 612357 |
Major Affective Disorder 8; MAFD8 |
| 612372 |
Major Affective Disorder 9; MAFD9 |
| 608520 |
Major Depressive Disorder 1 |
| 608691 |
Major Depressive Disorder 2 |
| 608516 |
Major Depressive Disorder; MDD (2 mouse models) |
| 142800 |
Major Histocompatibility Complex, Class I, A; HLA-A |
| 142830 |
Major Histocompatibility Complex, Class I, B; HLA-B |
| 154050 |
Major Intrinsic Protein of Lens Fiber; MIP (4 mouse models) |
| 609148 |
Malaria, Mild, Susceptibility to |
| 611162 |
Malaria, Susceptibility to (7 mouse models) |
| 248300 |
Mal De Meleda |
| 600122 |
Male Pseudohermaphroditism/Mental Retardation Syndrome, Verloes Type |
| 602248 |
Malignant Atrophic Papulosis |
| 145600 |
Malignant Hyperthermia, Susceptibility to, 1; MHS1 (2 mouse models) |
| 154275 |
Malignant Hyperthermia, Susceptibility to, 2 |
| 154276 |
Malignant Hyperthermia, Susceptibility to, 3 |
| 600467 |
Malignant Hyperthermia, Susceptibility to, 4 |
| 601887 |
Malignant Hyperthermia, Susceptibility to, 5 |
| 601888 |
Malignant Hyperthermia, Susceptibility to, 6 |
| 248350 |
Malocclusion and Short Stature |
| 154300 |
Malocclusion Due to Protuberant Upper Front Teeth |
| 248360 |
Malonyl-CoA Decarboxylase Deficiency |
| 189490 |
Malposition of Teeth with or without Hypodontia/Oligodontia |
| 613689 |
Mammary-Digital-Nail Syndrome; MDNS |
| 154370 |
Mammastatin |
| 607308 |
Mammographic Density |
| 248370 |
Mandibuloacral Dysplasia with Type A Lipodystrophy; MADA |
| 608612 |
Mandibuloacral Dysplasia with Type B Lipodystrophy; MADB |
| 610536 |
Mandibulofacial Dysostosis, Guion-Almeida Type; MFDGA |
| 604830 |
Mandibulofacial Dysostosis Syndrome, Bauru Type |
| 602562 |
Mandibulofacial Dysostosis with Macroblepharon and Macrostomia |
| 248400 |
Mandibulofacial Dysostosis with Mental Deficiency |
| 608257 |
Mandibulofacial Dysostosis with Ptosis, Autosomal Dominant |
| 248450 |
Manitoba Oculotrichoanal Syndrome; MOTA |
| 154570 |
Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type |
| 614372 |
Mannose-Binding Protein Deficiency |
| 248500 |
Mannosidosis, Alpha B, Lysosomal; MANSA (1 mouse model) |
| 248510 |
Mannosidosis, Beta A, Lysosomal; MANSB (1 mouse model) |
| 248600 |
Maple Syrup Urine Disease; MSUD (5 mouse models) |
| 154600 |
Marcus Gunn Phenomenon |
| 248700 |
Marden-Walker Syndrome |
| 248760 |
Marfanoid Habitus with Microcephaly and Glomerulonephritis |
| 609008 |
Marfanoid Habitus with Situs Inversus |
| 154750 |
Marfanoid Hypermobility Syndrome |
| 248770 |
Marfanoid Mental Retardation Syndrome, Autosomal |
| 154700 |
Marfan Syndrome; MFS (9 mouse models) |
| 248800 |
Marinesco-Sjogren Syndrome; MSS (1 mouse model) |
| 602535 |
Marshall-Smith Syndrome; MRSHSS |
| 154780 |
Marshall Syndrome; MRSHS (1 mouse model) |
| 212720 |
Martsolf Syndrome |
| 303350 |
MASA Syndrome (1 mouse model) |
| 613791 |
Masp2 Deficiency |
| 604308 |
MASS Syndrome |
| 154800 |
Mast Cell Disease (5 mouse models) |
| 154850 |
Masticatory Muscles, Hypertrophy of |
| 248900 |
Mast Syndrome |
| 606391 |
Maturity-Onset Diabetes of the Young; MODY (6 mouse models) |
| 613370 |
Maturity-Onset Diabetes of the Young, Type 10; MODY10 |
| 613375 |
Maturity-Onset Diabetes of the Young, Type 11; MODY11 |
| 125850 |
Maturity-Onset Diabetes of the Young, Type 1; MODY1 (1 mouse model) |
| 125851 |
Maturity-Onset Diabetes of the Young, Type 2; MODY2 (29 mouse models) |
| 600496 |
Maturity-Onset Diabetes of the Young, Type 3; MODY3 (3 mouse models) |
| 606392 |
Maturity-Onset Diabetes of the Young, Type 4; MODY4 (1 mouse model) |
| 606394 |
Maturity-Onset Diabetes of the Young, Type 6; MODY6 |
| 610508 |
Maturity-Onset Diabetes of the Young, Type 7; MODY7 |
| 609812 |
Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction; |
| 612225 |
Maturity-Onset Diabetes of the Young, Type 9; MODY9 |
| 155000 |
Maxillofacial Dysostosis |
| 155050 |
Maxillonasal Dysplasia, Binder Type |
| 277000 |
Mayer-Rokitansky-Kuster-Hauser Syndrome |
| 155100 |
May-Hegglin Anomaly; MHA |
| 174800 |
McCune-Albright Syndrome; MAS |
| 248950 |
McDonough Syndrome |
| 236700 |
McKusick-Kaufman Syndrome; MKKS |
| 300842 |
Mcleod Syndrome; MCLDS |
| 608978 |
Meacham Syndrome |
| 614644 |
Mean Platelet Volume Quantitative Trait Locus 4; MPVQTL4 |
| 614645 |
Mean Platelet Volume Quantitative Trait Locus 5; MPVQTL5 |
| 614646 |
Mean Platelet Volume Quantitative Trait Locus 6; MPVQTL6 |
| 155140 |
Meckel Diverticulum |
| 614175 |
Meckel Syndrome, Type 10; MKS10 |
| 249000 |
Meckel Syndrome, Type 1; MKS1 (2 mouse models) |
| 603194 |
Meckel Syndrome, Type 2; MKS2 |
| 607361 |
Meckel Syndrome, Type 3; MKS3 (1 mouse model) |
| 611134 |
Meckel Syndrome, Type 4; MKS4 |
| 611561 |
Meckel Syndrome, Type 5; MKS5 |
| 612284 |
Meckel Syndrome, Type 6; MKS6 |
| 267010 |
Meckel Syndrome, Type 7; MKS7 |
| 613885 |
Meckel Syndrome, Type 8; MKS8 |
| 614209 |
Meckel Syndrome, Type 9; MKS9 |
| 614665 |
Meconium Ileus |
| 155150 |
Median-Ulnar Nerve Communications |
| 155200 |
Mediosternal Depigmentation Line |
| 602199 |
Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency |
| 174000 |
Medullary Cystic Kidney Disease 1; MCKD1 (1 mouse model) |
| 603860 |
Medullary Cystic Kidney Disease 2; MCKD2 (1 mouse model) |
| 155255 |
Medulloblastoma; MDB (31 mouse models) |
| 249210 |
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome (1 mouse model) |
| 155310 |
Megaduodenum and/or Megacystis |
| 249230 |
Megaepiphyseal Dwarfism |
| 604004 |
Megalencephalic Leukoencephalopathy with Subcortical Cysts 1; MLC1 |
| 613925 |
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2A; MLC2A |
| 613926 |
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2b, Remitting, with or without Mental Retardation; MLC2B |
| 155350 |
Megalencephaly |
| 602501 |
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome; MCAP |
| 603387 |
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome; |
| 249240 |
Megalencephaly with Dysmyelination |
| 261100 |
Megaloblastic Anemia 1 |
| 613839 |
Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency |
| 249300 |
Megalocornea |
| 249310 |
Megalocornea-Mental Retardation Syndrome |
| 309300 |
Megalocornea; MGC1 |
| 155500 |
Megalodactyly |
| 612785 |
Megarbane-Jalkh Syndrome |
| 606527 |
Megarbane Syndrome |
| 224690 |
Meier-Gorlin Syndrome 1; MGORS1 |
| 613800 |
Meier-Gorlin Syndrome 2; MGORS2 |
| 613803 |
Meier-Gorlin Syndrome 3; MGORS3 |
| 613804 |
Meier-Gorlin Syndrome 4; MGORS4 |
| 613805 |
Meier-Gorlin Syndrome 5; MGORS5 |
| 155755 |
Melanoma-Astrocytoma Syndrome |
| 155600 |
Melanoma, Cutaneous Malignant, Susceptibility to, 1; CMM1 (3 mouse models) |
| 155601 |
Melanoma, Cutaneous Malignant, Susceptibility to, 2; CMM2 |
| 609048 |
Melanoma, Cutaneous Malignant, Susceptibility to, 3; CMM3 |
| 608035 |
Melanoma, Cutaneous Malignant, Susceptibility to, 4; CMM4 |
| 613099 |
Melanoma, Cutaneous Malignant, Susceptibility to, 5; CMM5 |
| 613972 |
Melanoma, Cutaneous Malignant, Susceptibility to, 6; CMM6 |
| 612263 |
Melanoma, Cutaneous Malignant, Susceptibility to, 7; CMM7 |
| 614456 |
Melanoma, Cutaneous Malignant, Susceptibility to, 8; CMM8 |
| 615134 |
Melanoma, Cutaneous Malignant, Susceptibility to, 9; CMM9 |
| 155700 |
Melanoma, Malignant Familial Intraocular |
| 606719 |
Melanoma-Pancreatic Cancer Syndrome |
| 155770 |
Melanoma Tumor Antigen Gp90 |
| 155720 |
Melanoma, Uveal (1 mouse model) |
| 606660 |
Melanoma, Uveal, Susceptibility to, 1 |
| 606661 |
Melanoma, Uveal, Susceptibility to, 2 |
| 249400 |
Melanosis, Neurocutaneous |
| 155800 |
Melanosis, Universal |
| 155900 |
Melkersson-Rosenthal Syndrome |
| 309350 |
Melnick-Needles Syndrome; MNS (1 mouse model) |
| 155950 |
Melorheostosis, Isolated |
| 305800 |
Membranoproliferative Glomerulonephritis, X-Linked (1 mouse model) |
| 155980 |
Membranous Cranial Ossification, Delayed |
| 614692 |
Membranous Nephropathy, Susceptibility To; MBNP |
| 156000 |
Meniere Disease |
| 607174 |
Meningioma, Familial, Susceptibility to (1 mouse model) |
| 606190 |
Meningioma, Radiation-Induced |
| 309400 |
Menkes Disease (5 mouse models) |
| 156190 |
Mental and Growth Retardation with Amblyopia |
| 603663 |
Mental Health Wellness 1 |
| 603664 |
Mental Health Wellness 2 |
| 300749 |
Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia; |
| 309480 |
Mental Retardation and Psoriasis |
| 613671 |
Mental Retardation, Anterior Maxillary Protrusion, and Strabismus; |
| 614256 |
Mental Retardation, Autosomal Dominant 10; MRD10 |
| 614257 |
Mental Retardation, Autosomal Dominant 11; MRD11 |
| 614562 |
Mental Retardation, Autosomal Dominant 12; MRD12 |
| 614563 |
Mental Retardation, Autosomal Dominant 13; MRD13 |
| 614607 |
Mental Retardation, Autosomal Dominant 14; MRD14 |
| 614608 |
Mental Retardation, Autosomal Dominant 15; MRD15 |
| 614609 |
Mental Retardation, Autosomal Dominant 16; MRD16 |
| 615009 |
Mental Retardation, Autosomal Dominant 17; MRD17 |
| 615074 |
Mental Retardation, Autosomal Dominant 18; MRD18 |
| 615075 |
Mental Retardation, Autosomal Dominant 19; MRD19 |
| 156200 |
Mental Retardation, Autosomal Dominant 1; MRD1 |
| 613443 |
Mental Retardation, Autosomal Dominant 20; MRD20 |
| 614113 |
Mental Retardation, Autosomal Dominant 2; MRD2 |
| 612580 |
Mental Retardation, Autosomal Dominant 3; MRD3 |
| 612581 |
Mental Retardation, Autosomal Dominant 4; MRD4 |
| 612621 |
Mental Retardation, Autosomal Dominant 5; MRD5 |
| 613970 |
Mental Retardation, Autosomal Dominant 6; MRD6 |
| 614104 |
Mental Retardation, Autosomal Dominant 7; MRD7 |
| 614254 |
Mental Retardation, Autosomal Dominant 8; MRD8 |
| 614255 |
Mental Retardation, Autosomal Dominant 9; MRD9 |
| 611096 |
Mental Retardation, Autosomal Recessive 10; MRT10 |
| 611097 |
Mental Retardation, Autosomal Recessive 11; MRT11 |
| 611090 |
Mental Retardation, Autosomal Recessive 12; MRT12 |
| 613192 |
Mental Retardation, Autosomal Recessive 13; MRT13 |
| 614020 |
Mental Retardation, Autosomal Recessive 14; MRT14 |
| 614202 |
Mental Retardation, Autosomal Recessive 15; MRT15 |
| 614208 |
Mental Retardation, Autosomal Recessive 16; MRT16 |
| 614207 |
Mental Retardation, Autosomal Recessive 17; MRT17 |
| 614249 |
Mental Retardation, Autosomal Recessive 18; MRT18 |
| 614343 |
Mental Retardation, Autosomal Recessive 19; MRT19 |
| 249500 |
Mental Retardation, Autosomal Recessive 1; MRT1 |
| 614344 |
Mental Retardation, Autosomal Recessive 23; MRT23 |
| 614345 |
Mental Retardation, Autosomal Recessive 24; MRT24 |
| 614346 |
Mental Retardation, Autosomal Recessive 25; MRT25 |
| 614340 |
Mental Retardation, Autosomal Recessive 27; MRT27 |
| 614347 |
Mental Retardation, Autosomal Recessive 28; MRT28 |
| 614333 |
Mental Retardation, Autosomal Recessive 29; MRT29 |
| 607417 |
Mental Retardation, Autosomal Recessive 2; MRT2 |
| 614342 |
Mental Retardation, Autosomal Recessive 30; MRT30 |
| 614329 |
Mental Retardation, Autosomal Recessive 31; MRT31 |
| 614339 |
Mental Retardation, Autosomal Recessive 32; MRT32 |
| 614341 |
Mental Retardation, Autosomal Recessive 33; MRT33 |
| 614499 |
Mental Retardation, Autosomal Recessive 34; MRT34 |
| 608443 |
Mental Retardation, Autosomal Recessive 3; MRT3 |
| 611107 |
Mental Retardation, Autosomal Recessive 4; MRT4 |
| 611091 |
Mental Retardation, Autosomal Recessive 5; MRT5 |
| 611092 |
Mental Retardation, Autosomal Recessive 6; MRT6 |
| 611093 |
Mental Retardation, Autosomal Recessive 7; MRT7 |
| 611094 |
Mental Retardation, Autosomal Recessive 8; MRT8 |
| 611095 |
Mental Retardation, Autosomal Recessive 9; MRT9 |
| 249630 |
Mental Retardation, Buenos Aires Type |
| 609313 |
Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma; MEDNIK |
| 300148 |
Mental Retardation, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity; MEHMO |
| 136630 |
Mental Retardation, Fra12a Type |
| 309580 |
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1; MRXHF1 |
| 609438 |
Mental Retardation, Keratoconus, Febrile Seizures, and Sinoatrial Block |
| 601352 |
Mental Retardation, Microcephaly, Epilepsy, and Coarse Face |
| 606242 |
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism |
| 606772 |
Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies |
| 602685 |
Mental Retardation, Severe, with Spasticity and Pigmentary Tapetoretinal Degeneration |
| 606220 |
Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations |
| 309620 |
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy; MRSD |
| 249599 |
Mental Retardation Syndrome, Belgian Type |
| 249600 |
Mental Retardation Syndrome, Mietens-Weber Type |
| 610156 |
Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis |
| 613670 |
Mental Retardation with Language Impairment and Autistic Features |
| 309555 |
Mental Retardation with Optic Atrophy, Deafness, and Seizures |
| 609037 |
Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature |
| 309640 |
Mental Retardation with Spastic Paraplegia |
| 309560 |
Mental Retardation with Spastic Paraplegia and Palmoplantar Hyperkeratosis |
| 300062 |
Mental Retardation, X-Linked 14; MRX14 |
| 300705 |
Mental Retardation, X-Linked 17; MRX17 |
| 300844 |
Mental Retardation, X-Linked 19; MRX19 |
| 309530 |
Mental Retardation, X-Linked 1; MRX1 |
| 300047 |
Mental Retardation, X-Linked 20; MRX20 |
| 300143 |
Mental Retardation, X-Linked 21; MRX21 |
| 300046 |
Mental Retardation, X-Linked 23; MRX23 |
| 300428 |
Mental Retardation, X-Linked 2; MRX2 |
| 300558 |
Mental Retardation, X-Linked 30; MRX30 |
| 309541 |
Mental Retardation, X-Linked 3; MRX3 (1 mouse model) |
| 300849 |
Mental Retardation, X-Linked 41; MRX41 |
| 300372 |
Mental Retardation, X-Linked 42; MRX42 |
| 300498 |
Mental Retardation, X-Linked 45; MRX45 |
| 300436 |
Mental Retardation, X-Linked 46; MRX46 |
| 300114 |
Mental Retardation, X-Linked 49; MRX49 |
| 300115 |
Mental Retardation, X-Linked 50; MRX50 |
| 300504 |
Mental Retardation, X-Linked 52; MRX52 |
| 300324 |
Mental Retardation, X-Linked 53; MRX53 |
| 300210 |
Mental Retardation, X-Linked 58; MRX58 |
| 300387 |
Mental Retardation, X-Linked 63; MRX63 |
| 300271 |
Mental Retardation, X-Linked 72; MRX72 |
| 300355 |
Mental Retardation, X-Linked 73; MRX73 |
| 300454 |
Mental Retardation, X-Linked 77; MRX77 |
| 300551 |
Mental Retardation, X-Linked 78; MRX78 |
| 300433 |
Mental Retardation, X-Linked 81; MRX81 |
| 300518 |
Mental Retardation, X-Linked 82; MRX82 |
| 300505 |
Mental Retardation, X-Linked 84; MRX84 |
| 300852 |
Mental Retardation, X-Linked 88; MRX88 |
| 300848 |
Mental Retardation, X-Linked 89; MRX89 |
| 300850 |
Mental Retardation, X-Linked 90; MRX90 |
| 300577 |
Mental Retardation, X-Linked 91; MRX91 |
| 300851 |
Mental Retardation, X-Linked 92; MRX92 |
| 300659 |
Mental Retardation, X-Linked 93; MRX93 |
| 300716 |
Mental Retardation, X-Linked 95; MRX95 |
| 300802 |
Mental Retardation, X-Linked 96; MRX96 |
| 300803 |
Mental Retardation, X-Linked 97; MRX97 |
| 309549 |
Mental Retardation, X-Linked 9; MRX9 |
| 309548 |
Mental Retardation, X-Linked, Associated with Fragile Site Fraxe |
| 300220 |
Mental Retardation, X-Linked, Syndromic 10; MRXS10 |
| 300238 |
Mental Retardation, X-Linked, Syndromic 11; MRXS11 |
| 309545 |
Mental Retardation, X-Linked, Syndromic 12; MRXS12 |
| 300055 |
Mental Retardation, X-Linked, Syndromic 13; MRXS13 |
| 300676 |
Mental Retardation, X-Linked, Syndromic 14; MRXS14 |
| 300858 |
Mental Retardation, X-Linked, Syndromic 17; MRXS17 |
| 300886 |
Mental Retardation, X-Linked, Syndromic 32; MRXS32 |
| 300218 |
Mental Retardation, X-Linked, Syndromic 7; MRXS7 |
| 300709 |
Mental Retardation, X-Linked, Syndromic 9; MRXS9 |
| 300243 |
Mental Retardation, X-Linked, Syndromic, Christianson Type; MRXSCH |
| 300861 |
Mental Retardation, X-Linked, Syndromic, Chudley-Schwartz Type; MRXSCS |
| 300534 |
Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type; MRXSCJ |
| 300630 |
Mental Retardation, X-Linked, Syndromic, Fried Type; MRXSF |
| 300423 |
Mental Retardation, X-Linked, Syndromic, Hedera Type; MRXSH |
| 300519 |
Mental Retardation, X-Linked, Syndromic, Martin-Probst Type; MRXSMP |
| 300860 |
Mental Retardation, X-Linked, Syndromic, Nascimento Type; MRXSN |
| 300799 |
Mental Retardation, X-Linked, Syndromic, Raymond Type; MRXSR |
| 309583 |
Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type; MRXSSR |
| 300706 |
Mental Retardation, X-Linked, Syndromic, Turner Type; MRXST |
| 300699 |
Mental Retardation, X-Linked, Syndromic, Wu Type; MRXSW |
| 300486 |
Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance (1 mouse model) |
| 300064 |
Mental Retardation, X-Linked, with Craniofacial Dysmorphism |
| 300419 |
Mental Retardation, X-Linked, with or without Seizures, Arx-Related; |
| 300123 |
Mental Retardation, X-Linked, with Panhypopituitarism Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency, |
| 300360 |
Mental Retardation, X-Linked, with Short Stature |
| 300354 |
Mental Retardation, X-Linked, with Short Stature, Hypogonadism, and Abnormal Gait |
| 156220 |
Meralgia Paraesthetica, Familial |
| 249650 |
Mercaptolactate-Cysteine Disulfiduria; MCDU |
| 249660 |
Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities |
| 249670 |
Mesoaxial Hexadactyly and Cardiac Malformation |
| 600383 |
Mesomelia-Synostoses Syndrome |
| 156230 |
Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type |
| 611886 |
Mesomelic Dysplasia, Camera Type |
| 156232 |
Mesomelic Dysplasia, Kantaputra Type |
| 605274 |
Mesomelic Dysplasia, Savarirayan Type |
| 249710 |
Mesomelic Limb Shortening and Bowing |
| 156240 |
Mesothelioma, Malignant; MESOM (4 mouse models) |
| 309630 |
Metacarpal 4-5 Fusion; MF4 |
| 156250 |
Metachondromatosis; METCDS |
| 156300 |
Metachromasia of Fibroblasts |
| 250100 |
Metachromatic Leukodystrophy (1 mouse model) |
| 156310 |
Metachromatic Leukodystrophy, Adult-Onset, with Normal Arylsulfatase A |
| 249900 |
Metachromatic Leukodystrophy Due to Saposin B Deficiency (1 mouse model) |
| 250215 |
Metaphyseal Acroscyphodysplasia |
| 613073 |
Metaphyseal Anadysplasia 2; MANDP2 |
| 156400 |
Metaphyseal Chondrodysplasia, Jansen Type (3 mouse models) |
| 250230 |
Metaphyseal Chondrodysplasia, Kaitila Type |
| 250300 |
Metaphyseal Chondrodysplasia, Pena Type |
| 156500 |
Metaphyseal Chondrodysplasia, Schmid Type; MCDS (1 mouse model) |
| 250400 |
Metaphyseal Chondrodysplasia, Spahr Type |
| 609989 |
Metaphyseal Chondrodysplasia with Cone-Shaped Epiphyses, Normal Hair, and Normal Hands |
| 250410 |
Metaphyseal Chondrodysplasia with Retinitis Pigmentosa |
| 250420 |
Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness |
| 250450 |
Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy |
| 605946 |
Metaphyseal Dysplasia, Braun-Tinschert Type |
| 156510 |
Metaphyseal Dysplasia with Maxillary Hypoplasia with or without Brachydactyly; |
| 250460 |
Metaphyseal Dysplasia without Hypotrichosis |
| 614875 |
Metaphyseal Enchondromatosis with D-2-Hydroxyglutaric Aciduria |
| 250500 |
Metaphyseal Modeling Abnormality, Skin Lesions, and Spastic Paraplegia |
| 608811 |
Metaphyseal Undermodeling, Spondylar Dysplasia, and Overgrowth |
| 156520 |
Metatarsus Varus, Type I |
| 156530 |
Metatropic Dysplasia |
| 250650 |
Methane Production |
| 250800 |
Methemoglobinemia Due to Deficiency of Methemoglobin Reductase |
| 250790 |
Methemoglobinemia Type IV |
| 250700 |
Methemoglobin Reductase Deficiency |
| 250850 |
Methionine Adenosyltransferase Deficiency (1 mouse model) |
| 250900 |
Methionine Malabsorption Syndrome |
| 250940 |
Methylcobalamin Deficiency, cblG Type |
| 614105 |
Methylmalonate Semialdehyde Dehydrogenase Deficiency; MMSDHD |
| 277400 |
Methylmalonic Aciduria and Homocystinuria, CblC Type |
| 277410 |
Methylmalonic Aciduria and Homocystinuria, CblD Type |
| 277380 |
Methylmalonic Aciduria and Homocystinuria, CblF Type |
| 614857 |
Methylmalonic Aciduria and Homocystinuria, Cblj Type; MAHCJ |
| 251100 |
Methylmalonic Aciduria, CblA Type |
| 251110 |
Methylmalonic Aciduria, CblB Type |
| 251000 |
Methylmalonic Aciduria Due to Methylmalonyl-CoA Mutase Deficiency (4 mouse models) |
| 613646 |
Methylmalonic Aciduria Due to Transcobalamin Receptor Defect |
| 251120 |
Methylmalonyl-Coa Epimerase Deficiency |
| 610377 |
Mevalonic Aciduria; MEVA |
| 210730 |
Microcephalic Osteodysplastic Primordial Dwarfism, Type III |
| 210720 |
Microcephalic Osteodysplastic Primordial Dwarfism, Type II; MOPD2 |
| 210710 |
Microcephalic Osteodysplastic Primordial Dwarfism, Type I; MOPD1 |
| 210700 |
Microcephalic Primordial Dwarfism, Montreal Type |
| 251190 |
Microcephalic Primordial Dwarfism, Toriello Type |
| 615095 |
Microcephaly 10, Primary, Autosomal Recessive; MCPH10 (1 mouse model) |
| 251200 |
Microcephaly 1, Primary, Autosomal Recessive; MCPH1 (1 mouse model) |
| 604317 |
Microcephaly 2, Primary, Autosomal Recessive, with or without Cortical Malformations; MCPH2 |
| 604804 |
Microcephaly 3, Primary, Autosomal Recessive; MCPH3 |
| 604321 |
Microcephaly 4, Primary, Autosomal Recessive; MCPH4 |
| 608716 |
Microcephaly 5, Primary, Autosomal Recessive; MCPH5 (2 mouse models) |
| 608393 |
Microcephaly 6, Primary, Autosomal Recessive; MCPH6 |
| 612703 |
Microcephaly 7, Primary, Autosomal Recessive; MCPH7 |
| 614673 |
Microcephaly 8, Primary, Autosomal Recessive; MCPH8 |
| 614852 |
Microcephaly 9, Primary, Autosomal Recessive; MCPH9 |
| 607196 |
Microcephaly, Amish Type; MCPHA (1 mouse model) |
| 251270 |
Microcephaly and Chorioretinopathy with or without Mental Retardation, Autosomal Recessive |
| 156580 |
Microcephaly, Autosomal Dominant |
| 614261 |
Microcephaly-Capillary Malformation Syndrome; MICCAP |
| 251220 |
Microcephaly-Cardiomyopathy |
| 614407 |
Microcephaly, Cerebellar Hypoplasia, and Cardiac Conduction Defect Syndrome; MCHCCD |
| 601355 |
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs |
| 601420 |
Microcephaly, Corpus Callosum Dysgenesis, and Cleft Lip/Palate |
| 156620 |
Microcephaly-Deafness Syndrome |
| 614231 |
Microcephaly, Epilepsy, and Diabetes Syndrome; MEDS |
| 603572 |
Microcephaly, Facial Abnormalities, Micromelia, and Mental Retardation |
| 612947 |
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance |
| 251300 |
Microcephaly, Hiatal Hernia, and Nephrotic Syndrome |
| 602555 |
Microcephaly, Macrotia, and Mental Retardation |
| 613680 |
Microcephaly, Mental Retardation, and Distinctive Facies, with Cardiac and Genitourinary Malformations |
| 251230 |
Microcephaly-Micromelia Syndrome |
| 613668 |
Microcephaly, Postnatal Progressive, with Seizures and Brain Atrophy |
| 601537 |
Microcephaly, Retinitis Pigmentosa, and Sutural Cataract |
| 603394 |
Microcephaly, Severe, with Skeletal Anomalies Including Posterior Rib-Gap Defects |
| 251250 |
Microcephaly with Cervical Spine Fusion Anomalies |
| 251240 |
Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia |
| 152950 |
Microcephaly with or without Chorioretinopathy, Lymphedema, or Mental Retardation; MCLMR |
| 603802 |
Microcephaly with Simplified Gyral Pattern |
| 251280 |
Microcephaly with Spastic Quadriplegia |
| 251400 |
Microcolon |
| 156600 |
Microcoria, Congenital |
| 156700 |
Microcornea, Glaucoma, and Absent Frontal Sinuses |
| 156810 |
Microgastria-Limb Reduction Defects Association; MLRD |
| 605013 |
Microhydranencephaly; MHAC |
| 156830 |
Micromelic Bone Dysplasia with Cloverleaf Skull |
| 251600 |
Microphthalmia, Isolated 1; MCOP1 |
| 610093 |
Microphthalmia, Isolated 2; MCOP2 |
| 611038 |
Microphthalmia, Isolated 3; MCOP3 |
| 613094 |
Microphthalmia, Isolated 4; MCOP4 |
| 611040 |
Microphthalmia, Isolated 5; MCOP5 |
| 613517 |
Microphthalmia, Isolated 6; MCOP6 (3 mouse models) |
| 613704 |
Microphthalmia, Isolated 7; MCOP7 |
| 615113 |
Microphthalmia, Isolated 8; MCOP8 |
| 156850 |
Microphthalmia, Isolated, with Cataract 1; MCOPCT1 |
| 212550 |
Microphthalmia, Isolated, with Cataract 2; MCOPCT2 |
| 302300 |
Microphthalmia, Isolated, with Cataract 3; MCOPCT3 |
| 610426 |
Microphthalmia, Isolated, with Cataract 4; MCOPCT4 |
| 300345 |
Microphthalmia, Isolated, with Coloboma 1; MCOPCB1 |
| 605738 |
Microphthalmia, Isolated, with Coloboma 2; MCOPCB2 |
| 610092 |
Microphthalmia, Isolated, with Coloboma 3; MCOPCB3 |
| 251505 |
Microphthalmia, Isolated, with Coloboma 4; MCOPCB4 |
| 611638 |
Microphthalmia, Isolated, with Coloboma 5; MCOPCB5 |
| 613703 |
Microphthalmia, Isolated, with Coloboma 6; MCOPCB6 |
| 614497 |
Microphthalmia, Isolated, with Coloboma 7; MCOPCB7 |
| 615145 |
Microphthalmia, Isolated, with Coloboma 9; MCOPCB9 |
| 156900 |
Microphthalmia, Isolated, with Corectopia; MCOPCR |
| 611222 |
Microphthalmia, Syndromic 10; MCOPS10 |
| 614402 |
Microphthalmia, Syndromic 11; MCOPS11 |
| 309800 |
Microphthalmia, Syndromic 1; MCOPS1 |
| 300166 |
Microphthalmia, Syndromic 2; MCOPS2 |
| 206900 |
Microphthalmia, Syndromic 3; MCOPS3 |
| 301590 |
Microphthalmia, Syndromic 4; MCOPS4 |
| 610125 |
Microphthalmia, Syndromic 5; MCOPS5 |
| 607932 |
Microphthalmia, Syndromic 6; MCOPS6 |
| 309801 |
Microphthalmia, Syndromic 7; MCOPS7 (9 mouse models) |
| 601349 |
Microphthalmia, Syndromic 8; MCOPS8 |
| 601186 |
Microphthalmia, Syndromic 9; MCOPS9 |
| 607597 |
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies |
| 251700 |
Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies |
| 206920 |
Microphthalmia with Limb Anomalies (2 mouse models) |
| 251750 |
Microspherophakia and/or Megalocornea, with Ectopia Lentis and with or without Secondary Glaucoma; MSPKA |
| 157151 |
Microspherophakia-Metaphyseal Dysplasia |
| 157150 |
Microspherophakia with Hernia |
| 600674 |
Microtia-Anotia (1 mouse model) |
| 612290 |
Microtia, Hearing Impairment, and Cleft Palate |
| 251800 |
Microtia with Meatal Atresia and Conductive Deafness |
| 611863 |
Microtia with Nasolacrimal Duct Imperforation and Eye Coloboma |
| 603933 |
Microvascular Complications of Diabetes, Susceptibility to, 1; MVCD1 |
| 612623 |
Microvascular Complications of Diabetes, Susceptibility to, 2; MVCD2 |
| 612624 |
Microvascular Complications of Diabetes, Susceptibility to, 3; MVCD3 |
| 612628 |
Microvascular Complications of Diabetes, Susceptibility to, 4; MVCD4 |
| 612633 |
Microvascular Complications of Diabetes, Susceptibility to, 5; MVCD5 |
| 612634 |
Microvascular Complications of Diabetes, Susceptibility to, 6; MVCD6 |
| 612635 |
Microvascular Complications of Diabetes, Susceptibility to, 7; MVCD7 |
| 608624 |
Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia |
| 601016 |
Midline Malformations, Multiple, with Limb Abnormalities and Hypopituitarism |
| 157200 |
Midphalangeal Hair |
| 141500 |
Migraine, Familial Hemiplegic, 1; FHM1 (3 mouse models) |
| 602481 |
Migraine, Familial Hemiplegic, 2; FHM2 |
| 609634 |
Migraine, Familial Hemiplegic, 3; FHM3 |
| 300125 |
Migraine, Familial Typical, Susceptibility to, 2 |
| 609179 |
Migraine with Aura, Susceptibility to, 7 |
| 609670 |
Migraine with Aura, Susceptibility to, 9 |
| 157300 |
Migraine with or without Aura, Susceptibility to, 1 |
| 610208 |
Migraine with or without Aura, Susceptibility to, 10 |
| 610209 |
Migraine with or without Aura, Susceptibility to, 11 |
| 611706 |
Migraine with or without Aura, Susceptibility to, 12; MGR12 |
| 613656 |
Migraine, with or without Aura, Susceptibility to, 13; MGR13 |
| 607498 |
Migraine with or without Aura, Susceptibility to, 3 |
| 607508 |
Migraine with or without Aura, Susceptibility to, 5 |
| 607516 |
Migraine with or without Aura, Susceptibility to, 6 |
| 609570 |
Migraine with or without Aura, Susceptibility to, 8 |
| 607501 |
Migraine without Aura, Susceptibility to, 4 |
| 309605 |
Miles-Carpenter X-Linked Mental Retardation Syndrome; MCS |
| 157400 |
Milia, Multiple Eruptive |
| 247200 |
Miller-Dieker Lissencephaly Syndrome; MDLS (6 mouse models) |
| 607552 |
Minicore Myopathy, Antenatal Onset, with Arthrogryposis |
| 255320 |
Minicore Myopathy with External Ophthalmoplegia (1 mouse model) |
| 157600 |
Mirror Movements 1; MRMV1 |
| 614508 |
Mirror Movements 2; MRMV2 |
| 276300 |
Mismatch Repair Cancer Syndrome; MMRCS |
| 252010 |
Mitochondrial Complex I Deficiency (2 mouse models) |
| 252011 |
Mitochondrial Complex II Deficiency |
| 124000 |
Mitochondrial Complex III Deficiency (1 mouse model) |
| 220110 |
Mitochondrial Complex IV Deficiency (2 mouse models) |
| 604273 |
Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 1; |
| 614052 |
Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 2; |
| 614053 |
Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 3; |
| 615084 |
Mitochondrial DNA Depletion Syndrome 11; MTDPS11 |
| 603041 |
Mitochondrial DNA Depletion Syndrome 1 (mngie Type); MTDPS1 |
| 609560 |
Mitochondrial DNA Depletion Syndrome 2 (myopathic Type); MTDPS2 (1 mouse model) |
| 251880 |
Mitochondrial DNA Depletion Syndrome 3 (hepatocerebral Type); MTDPS3 (1 mouse model) |
| 203700 |
Mitochondrial DNA Depletion Syndrome 4a (alpers Type); MTDPS4A |
| 613662 |
Mitochondrial DNA Depletion Syndrome 4b (mngie Type); MTDPS4B |
| 612073 |
Mitochondrial DNA Depletion Syndrome 5 (encephalomyopathic with Methylmalonic Aciduria); MTDPS5 |
| 256810 |
Mitochondrial DNA Depletion Syndrome 6 (hepatocerebral Type); MTDPS6 |
| 271245 |
Mitochondrial DNA Depletion Syndrome 7 (hepatocerebral Type); MTDPS7 |
| 612075 |
Mitochondrial DNA Depletion Syndrome 8a (encephalomyopathic Type with Renal Tubulopathy); MTDPS8A |
| 245400 |
Mitochondrial DNA Depletion Syndrome 9 (encephalomyopathic Type with Methylmalonic Aciduria); MTDPS9 |
| 600851 |
Mitochondrial Import-Stimulating Factor |
| 602252 |
Mitochondrial Intermembrane Space Protein Tim12, Yeast, Homolog of |
| 251900 |
Mitochondrial Myopathy (1 mouse model) |
| 540000 |
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes; MELAS |
| 500009 |
Mitochondrial Myopathy, Infantile, Transient; MMIT |
| 551000 |
Mitochondrial Myopathy, Lethal, Infantile; LIMM |
| 251945 |
Mitochondrial Myopathy with A Defect in Mitochondrial-Protein Transport |
| 500002 |
Mitochondrial Myopathy with Diabetes |
| 251950 |
Mitochondrial Myopathy with Lactic Acidosis |
| 610773 |
Mitochondrial Phosphate Carrier Deficiency |
| 614741 |
Mitochondrial Pyruvate Carrier Deficiency; MPYCD |
| 157800 |
Mitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones |
| 157700 |
Mitral Valve Prolapse, Familial; MVP |
| 607829 |
Mitral Valve Prolapse, Myxomatous 2; MMVP2 |
| 610840 |
Mitral Valve Prolapse, Myxomatous 3; MMVP3 |
| 254130 |
Miyoshi Muscular Dystrophy 1; MMD1 (4 mouse models) |
| 613318 |
Miyoshi Muscular Dystrophy 2; MMD2 |
| 613319 |
Miyoshi Muscular Dystrophy 3; MMD3 |
| 309840 |
Modifier, X-Linked, for Neurofunctional Defects |
| 157900 |
Moebius Syndrome; MBS |
| 252100 |
Mohr Syndrome |
| 304700 |
Mohr-Tranebjaerg Syndrome; MTS |
| 252150 |
Molybdenum Cofactor Deficiency (2 mouse models) |
| 157980 |
MOMO Syndrome |
| 158000 |
Monilethrix |
| 309850 |
Monoamine Oxidase A; MAOA (1 mouse model) |
| 252250 |
Monocyte Chemotactic Disorder |
| 613353 |
Mononeuropathy of the Median Nerve, Mild; MNMN |
| 158100 |
Monophalangy of Great Toe |
| 231630 |
Monosodium Glutamate Sensitivity |
| 252270 |
Monosomy 7 of Bone Marrow |
| 252300 |
Morquio Syndrome C |
| 257300 |
Mosaic Variegated Aneuploidy Syndrome 1; MVA1 |
| 614114 |
Mosaic Variegated Aneuploidy Syndrome 2; MVA2 |
| 158280 |
Motion Sickness |
| 600333 |
Motor Neuron Disease with Dementia and Ophthalmoplegia |
| 252320 |
Motor Neuropathy, Peripheral, with Dysautonomia |
| 235730 |
Mowat-Wilson Syndrome (1 mouse model) |
| 252350 |
Moyamoya Disease 1; MYMY1 |
| 607151 |
Moyamoya Disease 2; MYMY2 |
| 608796 |
Moyamoya Disease 3; MYMY3 |
| 300845 |
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism; MYMY4 |
| 614042 |
Moyamoya Disease 5; MYMY5 |
| 613342 |
Mseleni Joint Disease |
| 191900 |
Muckle-Wells Syndrome; MWS (5 mouse models) |
| 158310 |
Mucoepithelial Dysplasia, Hereditary |
| 252500 |
Mucolipidosis II Alpha/Beta (1 mouse model) |
| 252600 |
Mucolipidosis III Alpha/Beta |
| 252605 |
Mucolipidosis III Gamma |
| 252650 |
Mucolipidosis IV (2 mouse models) |
| 252700 |
Mucopolysaccharidoses, Unclassified Types |
| 309900 |
Mucopolysaccharidosis Type II (2 mouse models) |
| 252900 |
Mucopolysaccharidosis Type IIIA (1 mouse model) |
| 252920 |
Mucopolysaccharidosis Type IIIB (3 mouse models) |
| 252930 |
Mucopolysaccharidosis Type IIIC |
| 252940 |
Mucopolysaccharidosis Type IIID |
| 253000 |
Mucopolysaccharidosis Type IVA (2 mouse models) |
| 253010 |
Mucopolysaccharidosis Type IVB |
| 601492 |
Mucopolysaccharidosis Type IX (1 mouse model) |
| 253200 |
Mucopolysaccharidosis Type VI (3 mouse models) |
| 253220 |
Mucopolysaccharidosis Type VII (9 mouse models) |
| 253240 |
Mucus Inspissation of Respiratory Tract |
| 602849 |
Muenke Syndrome; MNKES (6 mouse models) |
| 158320 |
Muir-Torre Syndrome; MRTES (1 mouse model) |
| 253250 |
Mulibrey Nanism |
| 158330 |
Mullerian Aplasia and Hyperandrogenism |
| 235255 |
Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly |
| 601076 |
Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies; MURCS |
| 166300 |
Multicentric Carpotarsal Osteolysis Syndrome; MCTO |
| 253320 |
Multicore Myopathy with Mental Retardation, Short Stature, and Hypogonadotropic Hypogonadism |
| 143400 |
Multicystic Renal Dysplasia, Bilateral; MCRD (1 mouse model) |
| 231680 |
Multiple Acyl-CoA Dehydrogenase Deficiency; MADD |
| 614080 |
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1; MCAHS1 |
| 300868 |
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2; MCAHS2 |
| 607161 |
Multiple Congenital Anomalies Syndrome with Cloverleaf Skull |
| 614569 |
Multiple Enchondromatosis, Maffucci Type |
| 171400 |
Multiple Endocrine Neoplasia, Type IIA; MEN2A |
| 162300 |
Multiple Endocrine Neoplasia, Type IIB; MEN2B (2 mouse models) |
| 131100 |
Multiple Endocrine Neoplasia, Type I; MEN1 (6 mouse models) |
| 610755 |
Multiple Endocrine Neoplasia, Type IV; MEN4 |
| 601560 |
Multiple Epiphyseal Dysplasia with Robin Phenotype |
| 158345 |
Multiple Exostoses with Spastic Tetraparesis |
| 245600 |
Multiple Joint Dislocations, Short Stature, Craniofacial Dysmorphism, and Congenital Heart Defects |
| 605711 |
Multiple Mitochondrial Dysfunctions Syndrome 1; MMDS1 |
| 614299 |
Multiple Mitochondrial Dysfunctions Syndrome 2; MMDS2 |
| 265000 |
Multiple Pterygium Syndrome, Escobar Variant; EVMPS |
| 253290 |
Multiple Pterygium Syndrome, Lethal Type; LMPS |
| 312150 |
Multiple Pterygium Syndrome, X-Linked |
| 612594 |
Multiple Sclerosis, Susceptibility to, 2; MS2 |
| 612595 |
Multiple Sclerosis, Susceptibility to, 3; MS3 |
| 612596 |
Multiple Sclerosis, Susceptibility to, 4; MS4 |
| 614810 |
Multiple Sclerosis, Susceptibility to, 5; MS5 |
| 126200 |
Multiple Sclerosis, Susceptibility To; MS (16 mouse models) |
| 132800 |
Multiple Self-Healing Squamous Epithelioma, Susceptibility To; MSSE |
| 272200 |
Multiple Sulfatase Deficiency; MSD (1 mouse model) |
| 186500 |
Multiple Synostoses Syndrome 1; SYNS1 |
| 610017 |
Multiple Synostoses Syndrome 2; SYNS2 |
| 612961 |
Multiple Synostoses Syndrome 3; SYNS3 |
| 146500 |
Multiple System Atrophy; MSA (1 mouse model) |
| 613834 |
Multisystemic Smooth Muscle Dysfunction Syndrome |
| 611376 |
Mungan Syndrome; MGS |
| 158400 |
Muscle Cramps, Familial |
| 614160 |
Muscle Hypertrophy; MSLHP |
| 158500 |
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus |
| 158650 |
Muscular Atrophy, Malignant Neurogenic |
| 253590 |
Muscular Dystrophy, Adult-Onset, with Leukoencephalopathy |
| 158800 |
Muscular Dystrophy, Barnes Type |
| 300376 |
Muscular Dystrophy, Becker Type; BMD (1 mouse model) |
| 309930 |
Muscular Dystrophy, Cardiac Type |
| 604801 |
Muscular Dystrophy, Congenital, 1B; MDC1B |
| 613204 |
Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency (1 mouse model) |
| 613205 |
Muscular Dystrophy, Congenital, Lmna-Related (1 mouse model) |
| 602541 |
Muscular Dystrophy, Congenital, Megaconial Type; MDCMC (1 mouse model) |
| 607855 |
Muscular Dystrophy, Congenital Merosin-Deficient, 1A; MDC1A (9 mouse models) |
| 609456 |
Muscular Dystrophy, Congenital, Merosin-Positive |
| 253900 |
Muscular Dystrophy, Congenital, Producing Arthrogryposis |
| 603323 |
Muscular Dystrophy, Congenital, with Cerebellar Atrophy |
| 254000 |
Muscular Dystrophy, Congenital, with Infantile Cataract and Hypogonadism |
| 254100 |
Muscular Dystrophy, Congenital, with Rapid Progression |
| 601170 |
Muscular Dystrophy, Congenital, with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers |
| 310200 |
Muscular Dystrophy, Duchenne Type; DMD (20 mouse models) |
| 615041 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 10; MDDGA10 |
| 236670 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 1; MDDGA1 (1 mouse model) |
| 613150 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 2; MDDGA2 |
| 253280 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 3; MDDGA3 (2 mouse models) |
| 253800 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 4; MDDGA4 (5 mouse models) |
| 613153 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 5; MDDGA5 (1 mouse model) |
| 613154 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 6; MDDGA6 (2 mouse models) |
| 614643 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 7; MDDGA7 |
| 614830 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 8; MDDGA8 |
| 613155 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Mental Retardation), Type B, 1; MDDGB1 |
| 613156 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Mental Retardation), Type B, 2; MDDGB2 |
| 613151 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Mental Retardation), Type B, 3; MDDGB3 |
| 608840 |
Muscular Dystrophy-Dystroglycanopathy (congenital with Mental Retardation), Type B, 6; MDDGB6 (1 mouse model) |
| 606612 |
Muscular Dystrophy-Dystroglycanopathy (congenital with or without Mental Retardation), Type B, 5; MDDGB5 (1 mouse model) |
| 613152 |
Muscular Dystrophy-Dystroglycanopathy (congenital without Mental Retardation), Type B, 4; MDDGB4 (1 mouse model) |
| 609308 |
Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 1; MDDGC1 |
| 613158 |
Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 2; MDDGC2 |
| 613157 |
Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 3; MDDGC3 |
| 611588 |
Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 4; MDDGC4 |
| 607155 |
Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 5; MDDGC5 (1 mouse model) |
| 613818 |
Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 9; MDDGC9 (1 mouse model) |
| 309950 |
Muscular Dystrophy, Hemizygous Lethal Type |
| 159000 |
Muscular Dystrophy, Limb-Girdle, Type 1A; LGMD1A (1 mouse model) |
| 159001 |
Muscular Dystrophy, Limb-Girdle, Type 1B; LGMD1B (1 mouse model) |
| 607801 |
Muscular Dystrophy, Limb-Girdle, Type 1C; LGMD1C (2 mouse models) |
| 603511 |
Muscular Dystrophy, Limb-Girdle, Type 1E; LGMD1E |
| 608423 |
Muscular Dystrophy, Limb-Girdle, Type 1F; LGMD1F |
| 613530 |
Muscular Dystrophy, Limb-Girdle, Type 1H; LGMD1H |
| 253600 |
Muscular Dystrophy, Limb-Girdle, Type 2A; LGMD2A (2 mouse models) |
| 253601 |
Muscular Dystrophy, Limb-Girdle, Type 2B; LGMD2B (4 mouse models) |
| 253700 |
Muscular Dystrophy, Limb-Girdle, Type 2c; LGMD2C (2 mouse models) |
| 608099 |
Muscular Dystrophy, Limb-Girdle, Type 2D; LGMD2D (2 mouse models) |
| 604286 |
Muscular Dystrophy, Limb-Girdle, Type 2E; LGMD2E (2 mouse models) |
| 601287 |
Muscular Dystrophy, Limb-Girdle, Type 2F; LGMD2F (2 mouse models) |
| 601954 |
Muscular Dystrophy, Limb-Girdle, Type 2G; LGMD2G (1 mouse model) |
| 254110 |
Muscular Dystrophy, Limb-Girdle, Type 2H; LGMD2H (2 mouse models) |
| 608807 |
Muscular Dystrophy, Limb-Girdle, Type 2J; LGMD2J (3 mouse models) |
| 611307 |
Muscular Dystrophy, Limb-Girdle, Type 2L; LGMD2L |
| 613723 |
Muscular Dystrophy, Limb-Girdle, Type 2q; LGMD2Q |
| 310000 |
Muscular Dystrophy, Mabry Type |
| 310095 |
Muscular Dystrophy, Progressive Pectorodorsal |
| 159050 |
Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries |
| 600416 |
Muscular Dystrophy, Scapulohumeral |
| 254120 |
Muscular Hypertonia, Lethal |
| 159100 |
Muscular Hypoplasia, Congenital Universal, of Krabbe |
| 159300 |
Musical Perfect Pitch |
| 254150 |
Musk, Inability to Smell |
| 610452 |
Mutagen Sensitivity |
| 254190 |
Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors |
| 605809 |
Myasthenia, Familial Infantile, 1 |
| 254200 |
Myasthenia Gravis; MG |
| 607085 |
Myasthenia Gravis with Thymus Hyperplasia |
| 159400 |
Myasthenia, Limb-Girdle, Autoimmune |
| 254300 |
Myasthenia, Limb-Girdle, Familial (1 mouse model) |
| 614198 |
Myasthenic Syndrome, Congenital, Acetazolamide-Responsive |
| 608931 |
Myasthenic Syndrome, Congenital, Associated with Acetylcholine Receptor Deficiency (4 mouse models) |
| 254210 |
Myasthenic Syndrome, Congenital, Associated with Episodic Apnea |
| 608930 |
Myasthenic Syndrome, Congenital, Fast-Channel |
| 601462 |
Myasthenic Syndrome, Congenital, Slow-Channel; SCCMS (1 mouse model) |
| 610542 |
Myasthenic Syndrome, Congenital, with Tubular Aggregates 1; CMSTA1 |
| 614750 |
Myasthenic Syndrome, Congenital, with Tubular Aggregates 2; CMSTA2 |
| 613796 |
Mycobacterial and Viral Infections, Susceptibility to, Autosomal Recessive |
| 607948 |
Mycobacterium Tuberculosis, Susceptibility to |
| 607949 |
Mycobacterium Tuberculosis, Susceptibility to, 1 |
| 611046 |
Mycobacterium Tuberculosis, Susceptibility to, 2 |
| 612929 |
Mycobacterium Tuberculosis, Susceptibility to, 3 |
| 300259 |
Mycobacterium Tuberculosis, Susceptibility to, X-Linked |
| 254400 |
Mycosis Fungoides |
| 612260 |
Myd88 Deficiency; MYD88D |
| 159500 |
Myelinated Optic Nerve Fibers |
| 159550 |
Myelocerebellar Disorder |
| 600080 |
Myelocytic Leukemia-Like Syndrome, Familial, Chronic (6 mouse models) |
| 601347 |
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay |
| 614286 |
Myelodysplastic Syndrome; MDS (3 mouse models) |
| 254450 |
Myelofibrosis (4 mouse models) |
| 159555 |
Myeloid/Lymphoid or Mixed Lineage Leukemia Gene; MLL |
| 601308 |
Myeloid Tumor Suppressor |
| 310350 |
Myelolymphatic Insufficiency |
| 254500 |
Myeloma, Multiple (5 mouse models) |
| 159580 |
Myelopathy, Htlv-1-Associated; HAM (1 mouse model) |
| 254600 |
Myeloperoxidase Deficiency; MPOD (1 mouse model) |
| 254700 |
Myeloproliferative Disease, Autosomal Recessive (1 mouse model) |
| 131440 |
Myeloproliferative Disorder, Chronic, with Eosinophilia (1 mouse model) |
| 159595 |
Myeloproliferative Syndrome, Transient (2 mouse models) |
| 139210 |
Myhre Syndrome; MYHRS |
| 608446 |
Myocardial Infarction, Susceptibility to |
| 608557 |
Myocardial Infarction, Susceptibility to, 2 |
| 159900 |
Myoclonic Dystonia (2 mouse models) |
| 545000 |
Myoclonic Epilepsy Associated with Ragged-Red Fibers; MERRF |
| 604363 |
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders |
| 605021 |
Myoclonic Epilepsy, Familial Infantile; FIME |
| 159600 |
Myoclonic Epilepsy, Hartung Type |
| 608816 |
Myoclonic Epilepsy, Juvenile, Susceptibility to, 3; EJM3 |
| 611364 |
Myoclonic Epilepsy, Juvenile, Susceptibility to, 4; EJM4 |
| 254780 |
Myoclonic Epilepsy of Lafora (3 mouse models) |
| 254800 |
Myoclonic Epilepsy of Unverricht and Lundborg (1 mouse model) |
| 310370 |
Myoclonic Epilepsy, Progressive |
| 159700 |
Myoclonus and Ataxia |
| 159800 |
Myoclonus, Cerebellar Ataxia, and Deafness |
| 614937 |
Myoclonus, Familial Cortical; FCM |
| 268200 |
Myoglobinuria, Acute Recurrent, Autosomal Recessive |
| 160010 |
Myoglobinuria, Autosomal Dominant |
| 550500 |
Myoglobinuria, Recurrent |
| 614399 |
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset; |
| 609500 |
Myopathy, Autophagic Vacuolar, Infantile-Onset |
| 160150 |
Myopathy, Centronuclear, 1; CNM1 |
| 255200 |
Myopathy, Centronuclear, 2; CNM2 |
| 614408 |
Myopathy, Centronuclear, 3; CNM3 |
| 614807 |
Myopathy, Centronuclear, 4; CNM4 |
| 310400 |
Myopathy, Centronuclear, X-Linked; CNMX (1 mouse model) |
| 255300 |
Myopathy, Congenital (1 mouse model) |
| 612540 |
Myopathy, Congenital, Compton-North |
| 254940 |
Myopathy, Congenital Nonprogressive, with Moebius Sequence and Robin Sequence |
| 255310 |
Myopathy, Congenital, with Fiber-Type Disproportion; CFTD |
| 300580 |
Myopathy, Congenital, with Fiber-Type Disproportion, X-Linked; CFTDX |
| 160500 |
Myopathy, Distal, 1; MPD1 |
| 606070 |
Myopathy, Distal, 2; MPD2 |
| 610099 |
Myopathy, Distal, 3; MPD3 |
| 614065 |
Myopathy, Distal, 4; MPD4 |
| 614321 |
Myopathy, Distal, Tateyama Type; MPDT |
| 606768 |
Myopathy, Distal, with Anterior Tibial Onset; DMAT (2 mouse models) |
| 607569 |
Myopathy, Distal, with Early Respiratory Failure, Autosomal Dominant |
| 160300 |
Myopathy, Distal, with Onset in Infancy |
| 254960 |
Myopathy Due to Malate-Aspartate Shuttle Defect |
| 611705 |
Myopathy, Early-Onset, with Fatal Cardiomyopathy |
| 254950 |
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia |
| 255160 |
Myopathy, Hyaline Body, Autosomal Recessive |
| 600462 |
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1; MLASA1 |
| 613561 |
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2; MLASA2 |
| 613076 |
Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay |
| 601419 |
Myopathy, Myofibrillar, 1; MFM1 (2 mouse models) |
| 608810 |
Myopathy, Myofibrillar, 2, Mfm2 (2 mouse models) |
| 609200 |
Myopathy, Myofibrillar, 3; MFM3 (1 mouse model) |
| 609452 |
Myopathy, Myofibrillar, 4; MFM4 |
| 609524 |
Myopathy, Myofibrillar, 5; MFM5 |
| 612954 |
Myopathy, Myofibrillar 6, Mfm6 |
| 613869 |
Myopathy, Myofibrillar, Fatal Infantile Hypertonic, Alpha-B Crystallin-Related |
| 608358 |
Myopathy, Myosin Storage |
| 300718 |
Myopathy, Reducing Body, X-Linked, Childhood-Onset |
| 300717 |
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe |
| 182920 |
Myopathy, Spheroid Body (1 mouse model) |
| 160565 |
Myopathy, Tubular Aggregate |
| 255100 |
Myopathy with Abnormal Lipid Metabolism |
| 255140 |
Myopathy with Giant Abnormal Mitochondria |
| 255125 |
Myopathy with Lactic Acidosis, Hereditary; HML |
| 160570 |
Myopathy with Storage of Glycoproteins and Glycosaminoglycans |
| 310440 |
Myopathy, X-Linked, with Excessive Autophagy; MEAX |
| 300696 |
Myopathy, X-Linked, with Postural Muscle Atrophy; XMPMA |
| 609259 |
Myopia 10; MYP10 |
| 609994 |
Myopia 11, Autosomal Dominant; MYP11 |
| 609995 |
Myopia 12, Autosomal Dominant; MYP12 |
| 300613 |
Myopia 13, X-Linked; MYP13 |
| 610320 |
Myopia 14; MYP14 |
| 612717 |
Myopia 15, Autosomal Dominant; MYP15 |
| 612554 |
Myopia 16, Autosomal Dominant; MYP16 |
| 608367 |
Myopia 17, Autosomal Dominant; MYP17 |
| 255500 |
Myopia 18, Autosomal Recessive; MYP18 |
| 613969 |
Myopia 19, Autosomal Dominant; MYP19 |
| 310460 |
Myopia 1, X-Linked; MYP1 |
| 614166 |
Myopia 20, Autosomal Dominant; MYP20 |
| 614167 |
Myopia 21, Autosomal Dominant; MYP21 |
| 160700 |
Myopia 2, Autosomal Dominant; MYP2 (1 mouse model) |
| 603221 |
Myopia 3, Autosomal Dominant; MYP3 |
| 608474 |
Myopia 5, Autosomal Dominant; MYP5 |
| 608908 |
Myopia 6; MYP6 |
| 609256 |
Myopia 7; MYP7 |
| 609257 |
Myopia 8; MYP8 |
| 609258 |
Myopia 9; MYP9 |
| 614292 |
Myopia, High, with Cataract and Vitreoretinal Degeneration; MCVD |
| 255600 |
Myosclerosis, Autosomal Recessive |
| 160750 |
Myositis |
| 160800 |
Myotonia Congenita, Autosomal Dominant |
| 255700 |
Myotonia Congenita, Autosomal Recessive |
| 608390 |
Myotonia, Potassium-Aggravated |
| 255710 |
Myotonia with Skeletal Abnormalities and Mental Retardation |
| 160900 |
Myotonic Dystrophy 1; DM1 (14 mouse models) |
| 602668 |
Myotonic Dystrophy 2; DM2 |
| 160990 |
Myotonic Myopathy with Cylindrical Spirals |
| 300219 |
Myotubular Myopathy with Abnormal Genital Development |
| 255900 |
Myxedema |
| 613488 |
Myxoid Liposarcoma (1 mouse model) |
| 255960 |
Myxoma, Intracardiac |
Analysis Tools