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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 "M"

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OMIM IDHuman Disease
247990 MacDermot-Winter Syndrome
109150 Machado-Joseph Disease; MJD (15 mouse models)
606369 Macrocephaly and Epileptic Encephalopathy (1 mouse models)
605309 Macrocephaly/Autism Syndrome
153470 Macrocephaly, Benign Familial
614192 Macrocephaly, Macrosomia, Facial Dysmorphism Syndrome; MMFD
248000 Macrocephaly/Megalencephaly Syndrome, Autosomal Recessive; MGCPH
607131 Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies
600084 Macrocytosis, Familial (1 mouse models)
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
613075 Macs Syndrome
611488 Macular Degeneration, Age-Related, 10; ARMD10
611953 Macular Degeneration, Age-Related, 11; ARMD11
613784 Macular Degeneration, Age-Related, 12; ARMD12 (4 mouse models)
615439 Macular Degeneration, Age-Related, 13; ARMD13
615489 Macular Degeneration, Age-Related, 14; ARMD14
615591 Macular Degeneration, Age-Related, 15; ARMD15
603075 Macular Degeneration, Age-Related, 1; ARMD1 (4 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 (1 mouse models)
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
609628 Majeed Syndrome
125480 Major Affective Disorder 1; MAFD1 (1 mouse models)
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 (3 mouse models)
142830 Major Histocompatibility Complex, Class I, B; HLA-B
609148 Malaria, Mild, Susceptibility to
611162 Malaria, Susceptibility to (8 mouse models)
248300 Mal De Meleda; MDM
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
615381 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome; MDPL
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 (1 mouse models)
154570 Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type
614372 Mannose-Binding Protein Deficiency
248500 Mannosidosis, Alpha B, Lysosomal; MANSA (1 mouse models)
248510 Mannosidosis, Beta A, Lysosomal; MANSB (1 mouse models)
615135 Maple Syrup Urine Disease, Mild Variant; MSUDMV
248600 Maple Syrup Urine Disease; MSUD (5 mouse models)
154600 Marcus Gunn Phenomenon
248700 Marden-Walker Syndrome; MWKS
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 models)
602535 Marshall-Smith Syndrome; MRSHSS
154780 Marshall Syndrome; MRSHS (1 mouse models)
601346 Martinez-Frias Syndrome
212720 Martsolf Syndrome
303350 MASA Syndrome (1 mouse models)
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 models)
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 models)
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 (4 mouse models)
174800 McCune-Albright Syndrome; MAS
248950 McDonough Syndrome
236700 McKusick-Kaufman Syndrome; MKKS
300842 Mcleod Syndrome; MCLDS
608978 Meacham Syndrome
155140 Meckel Diverticulum
614175 Meckel Syndrome, Type 10; MKS10
615397 Meckel Syndrome, Type 11; MKS11
249000 Meckel Syndrome, Type 1; MKS1 (3 mouse models)
603194 Meckel Syndrome, Type 2; MKS2
607361 Meckel Syndrome, Type 3; MKS3 (2 mouse models)
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 models)
603860 Medullary Cystic Kidney Disease 2; MCKD2 (1 mouse models)
155255 Medulloblastoma; MDB (35 mouse models)
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, Autosomal Dominant
602501 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome; MCAP
603387 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1;
615937 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2;
615938 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3;
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
137550 Melanocytic Nevus Syndrome, Congenital; CMNS
155755 Melanoma-Astrocytoma Syndrome
615848 Melanoma, Cutaneous Malignant, Susceptibility to, 10; CMM10
155600 Melanoma, Cutaneous Malignant, Susceptibility to, 1; CMM1 (4 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 models)
606660 Melanoma, Uveal, Susceptibility to, 1
606661 Melanoma, Uveal, Susceptibility to, 2
249400 Melanosis, Neurocutaneous; NCMS
155800 Melanosis, Universal
615557 Melioidosis, Susceptibility to
155900 Melkersson-Rosenthal Syndrome
309350 Melnick-Needles Syndrome; MNS (1 mouse models)
155950 Melorheostosis, Isolated
305800 Membranoproliferative Glomerulonephritis, X-Linked (1 mouse models)
155980 Membranous Cranial Ossification, Delayed
614692 Membranous Nephropathy, Susceptibility To; MBNP
156000 Meniere Disease
607174 Meningioma, Familial, Susceptibility to (1 mouse models)
606190 Meningioma, Radiation-Induced
309400 Menkes Disease (5 mouse models)
156190 Mental and Growth Retardation with Amblyopia
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
615502 Mental Retardation, Autosomal Dominant 21; MRD21
612337 Mental Retardation, Autosomal Dominant 22; MRD22 (1 mouse models)
615761 Mental Retardation, Autosomal Dominant 23; MRD23
615828 Mental Retardation, Autosomal Dominant 24; MRD24
615834 Mental Retardation, Autosomal Dominant 26; MRD26
615866 Mental Retardation, Autosomal Dominant, 27; MRD27
615873 Mental Retardation, Autosomal Dominant, 28; MRD28
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
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
615162 Mental Retardation, Autosomal Recessive 35; MRT35
615286 Mental Retardation, Autosomal Recessive 36; MRT36
615493 Mental Retardation, Autosomal Recessive 37; MRT37
615516 Mental Retardation, Autosomal Recessive 38; MRT38
615541 Mental Retardation, Autosomal Recessive 39; MRT39
608443 Mental Retardation, Autosomal Recessive 3; MRT3
615599 Mental Retardation, Autosomal Recessive 40; MRT40
615637 Mental Retardation, Autosomal Recessive 41; MRT41
615802 Mental Retardation, Autosomal Recessive 42; MRT42
615817 Mental Retardation, Autosomal Recessive 43; MRT43
615942 Mental Retardation, Autosomal Recessive 44; MRT44
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
300923 Mental Retardation, X-Linked 100; MRX100
300928 Mental Retardation, X-Linked 101; MRX101
300062 Mental Retardation, X-Linked 14; MRX14
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
300849 Mental Retardation, X-Linked 41; MRX41 (1 mouse models)
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
300912 Mental Retardation, X-Linked 98; MRX98
300919 Mental Retardation, X-Linked 99; MRX99
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
304340 Mental Retardation, X-Linked, Syndromic 5; MRXS5
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
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 models)
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, (1 mouse models)
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; MMDK
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 models)
156310 Metachromatic Leukodystrophy, Adult-Onset, with Normal Arylsulfatase A
249900 Metachromatic Leukodystrophy Due to Saposin B Deficiency (1 mouse models)
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 models)
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 models)
250900 Methionine Malabsorption Syndrome
614105 Methylmalonate Semialdehyde Dehydrogenase Deficiency; MMSDHD
309541 Methylmalonic Acidemia and Homocysteinemia, Cblx Type
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 (5 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 models)
615414 Microcephaly 11, Primary, Autosomal Recessive; MCPH11
251200 Microcephaly 1, Primary, Autosomal Recessive; MCPH1 (1 mouse models)
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 models)
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
251230 Microcephaly-Micromelia Syndrome
613668 Microcephaly, Postnatal Progressive, with Seizures and Brain Atrophy
615760 Microcephaly, Progressive, with Seizures and Cerebral and Cerebellar Atrophy; MSCCA
601537 Microcephaly, Retinitis Pigmentosa, and Sutural Cataract
613402 Microcephaly, Seizures, and Developmental Delay; MCSZ
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
615458 Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus; MMCAT
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
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
615524 Microphthalmia, Syndromic 12; MCOPS12
300915 Microphthalmia, Syndromic 13; MCOPS13
615877 Microphthalmia, Syndromic 14; MCOPS14
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 models)
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 (5 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 models)
157600 Mirror Movements 1; MRMV1
614508 Mirror Movements 2; MRMV2
276300 Mismatch Repair Cancer Syndrome; MMRCS
615710 Mitchell-Riley Syndrome; MTCHRS
252010 Mitochondrial Complex I Deficiency (2 mouse models)
252011 Mitochondrial Complex II Deficiency
124000 Mitochondrial Complex III Deficiency, Nuclear Type 1; MC3DN1
615157 Mitochondrial Complex III Deficiency, Nuclear Type 2; MC3DN2
615158 Mitochondrial Complex III Deficiency, Nuclear Type 3; MC3DN3
615159 Mitochondrial Complex III Deficiency, Nuclear Type 4; MC3DN4
615160 Mitochondrial Complex III Deficiency, Nuclear Type 5; MC3DN5
615453 Mitochondrial Complex III Deficiency, Nuclear Type 6; MC3DN6
615824 Mitochondrial Complex III Deficiency, Nuclear Type 7; MC3DN7
615838 Mitochondrial Complex III Deficiency, Nuclear Type 8; MC3DN8
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;
615228 Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 4;
615084 Mitochondrial DNA Depletion Syndrome 11; MTDPS11
615418 Mitochondrial DNA Depletion Syndrome 12 (cardiomyopathic Type); MTDPS12
615471 Mitochondrial DNA Depletion Syndrome 13 (encephalomyopathic Type);
603041 Mitochondrial DNA Depletion Syndrome 1 (mngie Type); MTDPS1 (1 mouse models)
609560 Mitochondrial DNA Depletion Syndrome 2 (myopathic Type); MTDPS2 (1 mouse models)
251880 Mitochondrial DNA Depletion Syndrome 3 (hepatocerebral Type); MTDPS3 (1 mouse models)
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 or without 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 models)
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, Complementation Group A; MOCODA (1 mouse models)
252160 Molybdenum Cofactor Deficiency, Complementation Group B; MOCODB
615501 Molybdenum Cofactor Deficiency, Complementation Group C; MOCODC (1 mouse models)
157980 MOMO Syndrome
158000 Monilethrix; MNLIX
309850 Monoamine Oxidase A; MAOA (1 mouse models)
614894 Monocyte and Dendritic Cell Deficiency, Autosomal Recessive
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
615703 Morbid Obesity and Spermatogenic Failure; MOSPGF
252300 Morquio Syndrome C
257300 Mosaic Variegated Aneuploidy Syndrome 1; MVA1 (1 mouse models)
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; MOWS (1 mouse models)
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
615750 Moyamoya Disease 6 with Achalasia; MYMY6
613342 Mseleni Joint Disease
191900 Muckle-Wells Syndrome; MWS (5 mouse models)
158310 Mucoepithelial Dysplasia, Hereditary
252500 Mucolipidosis II Alpha/Beta (2 mouse models)
252600 Mucolipidosis III Alpha/Beta
252605 Mucolipidosis III Gamma
252650 Mucolipidosis IV (2 mouse models)
252700 Mucopolysaccharidoses, Unclassified Types
252900 Mucopolysaccharidosis, Type IIIA; MPS3A (1 mouse models)
252920 Mucopolysaccharidosis, Type IIIB; MPS3B (3 mouse models)
252930 Mucopolysaccharidosis, Type Iiic; MPS3C
252940 Mucopolysaccharidosis, Type Iiid; MPS3D
309900 Mucopolysaccharidosis, Type II; MPS2 (2 mouse models)
253000 Mucopolysaccharidosis, Type IVA; MPS4A (2 mouse models)
253010 Mucopolysaccharidosis Type IVB
601492 Mucopolysaccharidosis, Type IX; MPS9 (1 mouse models)
253220 Mucopolysaccharidosis, Type VII; MPS7 (9 mouse models)
253200 Mucopolysaccharidosis Type VI; MPS6 (3 mouse models)
253240 Mucus Inspissation of Respiratory Tract
602849 Muenke Syndrome; MNKES (6 mouse models)
158320 Muir-Torre Syndrome; MRTES (1 mouse models)
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
259600 Multicentric Osteolysis, Nodulosis, and Arthropathy; MONA (1 mouse models)
253320 Multicore Myopathy with Mental Retardation, Short Stature, and Hypogonadotropic Hypogonadism
143400 Multicystic Renal Dysplasia, Bilateral; MCRD (1 mouse models)
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
615398 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3; MCAHS3
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
615554 Multiple Fibroadenomas of the Breast; MFAB
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
615330 Multiple Mitochondrial Dysfunctions Syndrome 3; MMDS3
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 models)
186500 Multiple Synostoses Syndrome 1; SYNS1
610017 Multiple Synostoses Syndrome 2; SYNS2 (1 mouse models)
612961 Multiple Synostoses Syndrome 3; SYNS3
146500 Multiple System Atrophy 1, Susceptibility To; MSA1
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 models)
309930 Muscular Dystrophy, Cardiac Type
604801 Muscular Dystrophy, Congenital, 1B; MDC1B
613204 Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency (1 mouse models)
613205 Muscular Dystrophy, Congenital, Lmna-Related (1 mouse models)
602541 Muscular Dystrophy, Congenital, Megaconial Type; MDCMC (1 mouse models)
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 (21 mouse models)
615041 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 10; MDDGA10
615181 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 11; MDDGA11
615249 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 12; MDDGA12
615287 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 13; MDDGA13
615350 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 14; MDDGA14
236670 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 1; MDDGA1 (1 mouse models)
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 models)
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
615351 Muscular Dystrophy-Dystroglycanopathy (congenital with Mental Retardation), Type B, 14; MDDGB14
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 models)
606612 Muscular Dystrophy-Dystroglycanopathy (congenital with or without Mental Retardation), Type B, 5; MDDGB5 (1 mouse models)
613152 Muscular Dystrophy-Dystroglycanopathy (congenital without Mental Retardation), Type B, 4; MDDGB4 (1 mouse models)
615352 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 14; MDDGC14
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 (3 mouse models)
613818 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 9; MDDGC9 (1 mouse models)
309950 Muscular Dystrophy, Hemizygous Lethal Type
159000 Muscular Dystrophy, Limb-Girdle, Type 1A; LGMD1A (1 mouse models)
159001 Muscular Dystrophy, Limb-Girdle, Type 1B; LGMD1B (1 mouse models)
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 models)
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
615325 Muscular Dystrophy, Limb-Girdle, Type 2r; LGMD2R
615356 Muscular Dystrophy, Limb-Girdle, Type 2s; LGMD2S
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
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 models)
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 (2 mouse models)
615120 Myasthenic Syndrome, Congenital, with Pre- and Postsynaptic Defects;
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 (12 mouse models)
254450 Myelofibrosis (7 mouse models)
601308 Myeloid Tumor Suppressor
310350 Myelolymphatic Insufficiency
254500 Myeloma, Multiple (5 mouse models)
159580 Myelopathy, Htlv-1-Associated; HAM (1 mouse models)
254600 Myeloperoxidase Deficiency; MPOD (1 mouse models)
254700 Myeloproliferative Disease, Autosomal Recessive (1 mouse models)
131440 Myeloproliferative Disorder, Chronic, with Eosinophilia (1 mouse models)
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 models)
310370 Myoclonic Epilepsy, Progressive
159700 Myoclonus and Ataxia
159800 Myoclonus, Cerebellar Ataxia, and Deafness
614937 Myoclonus, Familial Cortical; FCM
228550 Myofibromatosis, Infantile, 1; IMF1
615293 Myofibromatosis, Infantile, 2; IMF2
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
615959 Myopathy, Centronuclear, 5; CNM5
310400 Myopathy, Centronuclear, X-Linked; CNMX (1 mouse models)
255300 Myopathy, Congenital (1 mouse models)
612540 Myopathy, Congenital, Compton-North; MYPCN
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
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
615511 Myopathy Due to Myoadenylate Deaminase Deficiency; MMDD
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 models)
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 models)
160565 Myopathy, Tubular Aggregate, 1; TAM1
615883 Myopathy, Tubular Aggregate, 2; TAM2
255100 Myopathy with Abnormal Lipid Metabolism
615673 Myopathy with Extrapyramidal Signs; MPXPS
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
615420 Myopia 22, Autosomal Dominant; MYP22
615431 Myopia 23, Autosomal Recessive; MYP23
615946 Myopia 24, Autosomal Dominant; MYP24
160700 Myopia 2, Autosomal Dominant; MYP2 (1 mouse models)
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 (1 mouse models)
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 (17 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 models)
255960 Myxoma, Intracardiac

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/09/2014
MGI 5.19
The Jackson Laboratory