Disease Name Symbol Acronym
Machado-Joseph Disease MCH002 SCA3
Machado-Joseph Disease Type 1 MCH012
Machado-Joseph Disease Type 2 MCH014
Machado-Joseph Disease Type 3 MCH013
Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation MCR321
Macrocephaly, Macrosomia, and Facial Dysmorphism Syndrome MCR353
Macrocephaly/autism Syndrome MCR096
Macrocephaly/megalencephaly Syndrome, Autosomal Recessive MCR237
Macrocytic Anemia MCR017
Macrodactyly of Fingers, Unilateral MCR188
Macrodactyly of Toes MCR185
Macrodactyly of Toes, Unilateral MCR190
Macroglobulinemia MCR004
Macroglobulinemia, Waldenstrom 1 MCR161
Macroglobulinemia, Waldenstrom 2 MCR162
Macroglossia MCR037
Macrophage Activation Syndrome MCR225
Macrophthalmia, Colobomatous, with Microcornea MCR317
Macrostomia, Isolated MCR302
Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss MCR359
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related MCR125
Macrozoospermia MCR265
Macs Syndrome MCS006
Macular Amyloidosis MCL047
Macular Degeneration, Age-Related, 1 MCL042
Macular Degeneration, Age-Related, 10 MCL030
Macular Degeneration, Age-Related, 11 MCL032
Macular Degeneration, Age-Related, 12 MCL051
Macular Degeneration, Age-Related, 13 MCL052
Macular Degeneration, Age-Related, 14 MCL078
Macular Degeneration, Age-Related, 15 MCL065
Macular Degeneration, Age-Related, 2 MCL043
Macular Degeneration, Age-Related, 4 MCL038
Macular Degeneration, Age-Related, 5 MCL077
Macular Degeneration, Age-Related, 6 MCL036
Macular Degeneration, Age-Related, 7 MCL041
Macular Degeneration, Age-Related, 8 MCL039
Macular Degeneration, Age-Related, 9 MCL044
Macular Degeneration, Early-Onset MCL058
Macular Degeneration, X-Linked Atrophic MCL029
Macular Dystrophy with Central Cone Involvement MCL057
Macular Dystrophy, Concentric Annular MCL018
Macular Dystrophy, Corneal MCL075
Macular Dystrophy, Dominant Cystoid MCL027
Macular Dystrophy, Patterned, 1 MCL059
Macular Dystrophy, Patterned, 2 MCL071
Macular Dystrophy, Patterned, 3 MCL070
Macular Dystrophy, Retinal, 1, North Carolina Type MCL069
Macular Dystrophy, Retinal, 2 MCL035
Macular Dystrophy, Retinal, 3 MCL026
Macular Dystrophy, Vitelliform, 1 MCL073
Macular Dystrophy, Vitelliform, 2 MCL066
Macular Dystrophy, Vitelliform, 3 MCL060
Macular Dystrophy, Vitelliform, 4 MCL061
Macular Dystrophy, Vitelliform, 5 MCL056
Macular Holes MCL003
Macular Retinal Edema MCL006
Macular Telangiectasia Type 2 MCL079
Madelung Deformity MDL024
Madras Motor Neuron Disease MDR004
Main Bronchus Cancer MNB001
Majeed Syndrome MJD001
Major Affective Disorder 1 MJR007 MD1
Major Affective Disorder 2 MJR008
Major Affective Disorder 3 MJR021
Major Affective Disorder 4 MJR004
Major Affective Disorder 5 MJR006
Major Affective Disorder 6 MJR003
Major Affective Disorder 7 MJR023
Major Affective Disorder 8 MJR022
Major Affective Disorder 9 MJR024
Major Depressive Disorder MJR001
Major Depressive Disorder 1 MJR013
Major Depressive Disorder 2 MJR014
Mal De Meleda MLD006
Malaria MLR004
Malaria, Mild MLR020
Male Infertility MLN007
Male Reproductive Organ Benign Neoplasm MLR005
Male Reproductive Organ Cancer MLR006
Male Reproductive System Disease MLR007
Maleylacetoacetate Isomerase Deficiency MLY011
Maligant Granulosa Cell Tumor of the Ovary MLG155
Malignant Anus Melanoma MLG038
Malignant Atrophic Papulosis MLG141
Malignant Biphasic Mesothelioma MLG011
Malignant Choroid Melanoma MLG061
Malignant Ciliary Body Melanoma MLG062
Malignant Conjunctival Melanoma MLG142
Malignant Cylindroma MLG087
Malignant Dermis Tumor MLG063
Malignant Ectomesenchymoma MLG133
Malignant Ependymoma MLG064
Malignant Epithelial Mesothelioma MLG012
Malignant Epithelial Tumor of Salivary Glands MLG134
Malignant Essential Hypertension MLG039
Malignant Fibrous Histiocytoma of Bone MLG014
Malignant Fibroxanthoma MLG065
Malignant Germ Cell Tumor MLG088
Malignant Giant Cell Tumor MLG067
Malignant Giant Cell Tumor of Soft Parts MLG018
Malignant Glandular Tumor of Peripheral Nerve Sheath MLG051
Malignant Glioma MLG068
Malignant Granular Cell Myoblastoma MLG032
Malignant Hemangioma MLG144
Malignant Histiocytosis MLG054
Malignant Hypertension MLG069
Malignant Hyperthermia MLG056
Malignant Hyperthermia 1 MLG147
Malignant Hyperthermia 2 MLG148
Malignant Hyperthermia 3 MLG149
Malignant Hyperthermia 4 MLG150
Malignant Hyperthermia 5 MLG151
Malignant Hyperthermia 6 MLG152
Malignant Hyperthermia of Anesthesia MLG143
Malignant Hyperthermia Susceptibility MLG086
Malignant Iris Melanoma MLG070
Malignant Leptomeningeal Tumor MLG071
Malignant Leydig Cell Tumor MLG072
Malignant Mesenchymoma MLG074
Malignant Migrating Partial Seizures of Infancy MLG120
Malignant Mixed Mullerian Tumor MLG098
Malignant Otitis Externa MLG042
Malignant Ovarian Brenner Tumor MLG053
Malignant Ovarian Cyst MLG033
Malignant Ovarian Surface Epithelial-Stromal Neoplasm MLG076
Malignant Peripheral Nerve Sheath Tumor MLG077
Malignant Peritoneal Mesothelioma MLG002
Malignant Pineal Area Germ Cell Neoplasm MLG078
Malignant Pleural Mesothelioma MLG079
Malignant Renovascular Hypertension MLG003
Malignant Secondary Hypertension MLG080
Malignant Sertoli Cell Tumor MLG022
Malignant Sertoli-Leydig Cell Tumor of the Ovary MLG154
Malignant Skin Fibrous Histiocytoma MLG007
Malignant Spindle Cell Melanoma MLG005
Malignant Spiradenoma MLG036
Malignant Struma Ovarii MLG059
Malignant Syringoma MLG049
Malignant Teratoma MLG081
Malignant Triton Tumor MLG041
Malonyl-Coa Decarboxylase Deficiency MLN011
Mammary Paget's Disease MMM001
Mammary-Digital-Nail Syndrome MMM002
Mammographic Density MMM006
Man1b1-Cdg MN1002
Mandibular Cancer MND001
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome MND021
Mandibuloacral Dysplasia with Type a Lipodystrophy MND003
Mandibuloacral Dysplasia with Type B Lipodystrophy MND002
Mandibulofacial Dysostosis with Alopecia MND025
Mandibulofacial Dysostosis with Mental Retardation MND028
Mandibulofacial Dysostosis, Guion-Almeida Type MND020
Manitoba Oculotrichoanal Syndrome MNT006
Mannose-Binding Lectin Deficiency MNN034
Mannosidosis MNN018
Mannosidosis, Alpha B, Lysosomal MNN047
Mannosidosis, Beta a, Lysosomal MNN019
Mansonelliasis MNS001
Mantle Cell Lymphoma MNT001
Maple Syrup Urine Disease MPL001
Maple Syrup Urine Disease, Mild Variant MPL011
Marantic Endocarditis MRN001
Marasmus MRS001
Marburg Hemorrhagic Fever MRB001
Marcus Gunn Phenomenon MRC002
Marden Walker Like Syndrome MRD001
Marden-Walker Syndrome MRD002
Marek Disease MRK002
Marfan Lipodystrophy Syndrome MRF019
Marfan Syndrome MRF001
Marginal Zone B-Cell Lymphoma MRG003
Marie Unna Congenital Hypotrichosis MRN005
Marinesco-Sjogren Syndrome MRN003
Marshall Syndrome MRS002
Marshall-Smith Syndrome MRS004
Marsili Syndrome MRS009
Martinez-Frias Syndrome MRT009
Martsolf Syndrome MRT007
Masa Syndrome MSS001
Masp2 Deficiency MSP001
Mass Syndrome MSS002
Mast Cell Activation Syndrome MST020
Mast Cell Disease MST017
Mast Cell Neoplasm MST004
Mast Syndrome MST006
Mast-Cell Leukemia MST002
Mast-Cell Sarcoma MST001
Masters-Allen Syndrome MST003
Mastitis MST005
Mastoiditis MST019
Maternal Uniparental Disomy of Chromosome 1 MTR051
Maternal Uniparental Disomy of Chromosome 16 MTR067
Maternal Uniparental Disomy of Chromosome 22 MTR064
Maternal Uniparental Disomy of Chromosome 4 MTR062
Maternally-Inherited Cardiomyopathy and Hearing Loss MTR049
Maternally-Inherited Progressive External Ophthalmoplegia MTR058
Maternally-Inherited Spastic Paraplegia MTR059
Mature B-Cell Neoplasm MTR008
Mature Cataract MTR001
Mature Teratoma MTR010
Mature Teratoma of the Ovary MTR011
Maturity-Onset Diabetes of the Young MTR004
Maturity-Onset Diabetes of the Young, Type 1 MTR018 MODY1
Maturity-Onset Diabetes of the Young, Type 10 MTR044
Maturity-Onset Diabetes of the Young, Type 11 MTR039
Maturity-Onset Diabetes of the Young, Type 13 MTR075
Maturity-Onset Diabetes of the Young, Type 14 MTR074
Maturity-Onset Diabetes of the Young, Type 2 MTR019 MODY2
Maturity-Onset Diabetes of the Young, Type 3 MTR020
Maturity-Onset Diabetes of the Young, Type 4 MTR021
Maturity-Onset Diabetes of the Young, Type 6 MTR023
Maturity-Onset Diabetes of the Young, Type 7 MTR024
Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction MTR082
Maturity-Onset Diabetes of the Young, Type 9 MTR026
Maxillary Sinus Adenoid Cystic Carcinoma MXL002
Maxillary Sinus Cancer MXL008
Maxillary Sinus Squamous Cell Carcinoma MXL004
Maxillary Sinusitis MXL015
Maxillonasal Dysplasia, Binder Type MXL016
May-Thurner Syndrome MYT019
Mayer-Rokitansky-Kuster-Hauser Syndrome MYR002
Mazabraud Syndrome MZB001
Mbd5 Haploinsufficiency MBD001
Mccune-Albright Syndrome MCC012
Mckusick-Kaufman Syndrome MCK005
Mcleod Syndrome MCL009
Mda5 Deficiency MD5001
Meacham Syndrome MCH011
Mean Platelet Volume Quantitative Trait Locus 1 MNP014
Mean Platelet Volume Quantitative Trait Locus 2 MNP015
Mean Platelet Volume Quantitative Trait Locus 3 MNP016
Mean Platelet Volume Quantitative Trait Locus 4 MNP019
Mean Platelet Volume Quantitative Trait Locus 5 MNP020
Mean Platelet Volume Quantitative Trait Locus 6 MNP021
Measles MSL001
Mechanical Ectropion MCH001
Meckel Diverticulum MCK029
Meckel Syndrome 12 MCK026
Meckel Syndrome 13 MCK028
Meckel Syndrome, Type 1 MCK013
Meckel Syndrome, Type 10 MCK035
Meckel Syndrome, Type 11 MCK020
Meckel Syndrome, Type 2 MCK031
Meckel Syndrome, Type 3 MCK032
Meckel Syndrome, Type 4 MCK033
Meckel Syndrome, Type 5 MCK014
Meckel Syndrome, Type 6 MCK012
Meckel Syndrome, Type 7 MCK030
Meckel Syndrome, Type 8 MCK034
Meckel Syndrome, Type 9 MCK036
Meconium Aspiration Syndrome MCN007
Meconium Ileus MCN017
Med13l Haploinsufficiency Syndrome MD1003
Med23 MD2001
Median Arcuate Ligament Syndrome MDN008
Median Neuropathy MDN002
Median Rhomboid Glossitis MDN001
Mediastinal Cancer MDS018
Mediastinal Gray Zone Lymphoma MDS006
Mediastinal Lipomatosis MDS003
Mediastinal Malignant Lymphoma MDS019
Mediastinitis MDS022
Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency MDM001
Medullary Cystic Kidney Disease 1 MDL008
Medullary Cystic Kidney Disease 2 MDL021
Medullary Sponge Kidney MDL009
Medulloblastoma MDL005
Medulloepithelioma MDL002
Medullomyoblastoma MDL003
Meester-Loeys Syndrome MST021
Megacolon MGC001
Megaesophagus MGS001
Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) MGK005
Megakaryocytic Leukemia MGK001
Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 MGL009
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a MGL010
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2b, Remitting, with or Without Mental Retardation MGL011
Megalencephaly MGL013
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome MGL038
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 MGL030
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2 MGL028
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3 MGL029
Megaloblastic Anemia MGL001
Megaloblastic Anemia 1 MGL018
Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency MGL012
Megalocornea MGL003
Mehmo Syndrome MHM001
Meibomian Cyst MBM001
Meier-Gorlin Syndrome 1 MRG008
Meier-Gorlin Syndrome 2 MRG009
Meier-Gorlin Syndrome 3 MRG010
Meier-Gorlin Syndrome 4 MRG011
Meier-Gorlin Syndrome 5 MRG012
Meier-Gorlin Syndrome 6 MRG014
Meier-Gorlin Syndrome 7 MRG015
Meier-Gorlin Syndrome 8 MRG016
Melancholia MLN003
Melanoacanthoma MLN005
Melanocytic Nevus Syndrome, Congenital MLN065
Melanoma MLN008
Melanoma Metastasis MLN013
Melanoma of Soft Tissue MLN064
Melanoma-Associated Retinopathy MLN046
Melanoma-Astrocytoma Syndrome MLN070
Melanoma-Pancreatic Cancer Syndrome MLN047
Melanoma, Cutaneous Malignant 1 MLN066
Melanoma, Cutaneous Malignant 10 MLN055
Melanoma, Cutaneous Malignant 2 MLN067
Melanoma, Cutaneous Malignant 3 MLN075
Melanoma, Cutaneous Malignant 4 MLN074
Melanoma, Cutaneous Malignant 5 MLN076
Melanoma, Cutaneous Malignant 6 MLN042
Melanoma, Cutaneous Malignant 7 MLN040
Melanoma, Cutaneous Malignant 8 MLN043
Melanoma, Cutaneous Malignant 9 MLN077
Melanoma, Uveal MLN069
Melanoma, Uveal 1 MLN039
Melanoma, Uveal 2 MLN041
Melanomatosis MLN002
Melanosis, Neurocutaneous MLN073
Melanotic Medulloblastoma MLN004
Melanotic Neurilemmoma MLN009
Melanotic Neuroectodermal Tumor MLN001
Melioidosis MLD001
Melkersson-Rosenthal Syndrome MLK003
Melnick-Needles Syndrome MLN014
Melon Allergy MLN063
Melorheostosis MLR003
Melorheostosis with Osteopoikilosis MLR010
Membranoproliferative Glomerulonephritis MMB001
Membranous Nephropathy MMB011
Memory Quantitative Trait Locus MMR005
Menarche, Age at, Quantitative Trait Locus 1 MNR013
Menarche, Age at, Quantitative Trait Locus 2 MNR014
Menarche, Age at, Quantitative Trait Locus 3 MNR015
Mend Syndrome MND023
Meniere Disease MNR012
Meningeal Melanocytoma MNN001
Meningeal Melanoma MNN010
Meningeal Melanomatosis MNN008
Meninges Hemangiopericytoma MNN006
Meninges Sarcoma MNN011
Meningioma, Familial MNN043
Meningioma, Radiation-Induced MNN042
Meningitis MNN013
Meningitis and Encephalitis MNN024
Meningocele MNN007
Meningococcal Infection MNN020
Meningococcal Meningitis MNN032
Meningococcemia MNN021
Meningoencephalitis MNN009
Meningoencephalocele MNN022
Meningothelial Meningioma MNN004
Meningovascular Neurosyphilis MNN005
Menkes Disease MNK001
Menopause, Natural, Age at, Quantitative Trait Locus 1 MNP013
Menopause, Natural, Age at, Quantitative Trait Locus 2 MNP017
Menopause, Natural, Age at, Quantitative Trait Locus 4 MNP018
Mental Depression MNT002
Mental Health Wellness 1 MNT312
Mental Health Wellness 2 MNT313
Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects MNT266
Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia MNT046
Mental Retardation with Language Impairment and with or Without Autistic Features MNT237
Mental Retardation with Optic Atrophy, Deafness, and Seizures MNT308
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 MNT309
Mental Retardation, Anterior Maxillary Protrusion, and Strabismus MNT118
Mental Retardation, Autosomal Dominant 10 MNT186
Mental Retardation, Autosomal Dominant 11 MNT184
Mental Retardation, Autosomal Dominant 13 MNT143
Mental Retardation, Autosomal Dominant 18 MNT157
Mental Retardation, Autosomal Dominant 19 MNT159
Mental Retardation, Autosomal Dominant 20 MNT319
Mental Retardation, Autosomal Dominant 21 MNT179
Mental Retardation, Autosomal Dominant 22 MNT158
Mental Retardation, Autosomal Dominant 23 MNT211
Mental Retardation, Autosomal Dominant 24 MNT214
Mental Retardation, Autosomal Dominant 26 MNT212
Mental Retardation, Autosomal Dominant 27 MNT322
Mental Retardation, Autosomal Dominant 29 MNT222
Mental Retardation, Autosomal Dominant 30 MNT219
Mental Retardation, Autosomal Dominant 31 MNT226
Mental Retardation, Autosomal Dominant 32 MNT241
Mental Retardation, Autosomal Dominant 33 MNT240
Mental Retardation, Autosomal Dominant 34 MNT238
Mental Retardation, Autosomal Dominant 35 MNT239
Mental Retardation, Autosomal Dominant 36 MNT245
Mental Retardation, Autosomal Dominant 38 MNT246
Mental Retardation, Autosomal Dominant 39 MNT236
Mental Retardation, Autosomal Dominant 40 MNT242
Mental Retardation, Autosomal Dominant 41 MNT272
Mental Retardation, Autosomal Dominant 42 MNT262
Mental Retardation, Autosomal Dominant 43 MNT280
Mental Retardation, Autosomal Dominant 44 MNT273
Mental Retardation, Autosomal Dominant 45 MNT286
Mental Retardation, Autosomal Dominant 46 MNT278
Mental Retardation, Autosomal Dominant 47 MNT279
Mental Retardation, Autosomal Dominant 48 MNT323
Mental Retardation, Autosomal Dominant 49 MNT324
Mental Retardation, Autosomal Dominant 50 MNT326
Mental Retardation, Autosomal Dominant 51 MNT327
Mental Retardation, Autosomal Dominant 52 MNT328
Mental Retardation, Autosomal Dominant 53 MNT329
Mental Retardation, Autosomal Dominant 54 MNT330
Mental Retardation, Autosomal Dominant 55, with Seizures MNT331
Mental Retardation, Autosomal Dominant 56 MNT332
Mental Retardation, Autosomal Dominant 6, with or Without Seizures MNT320
Mental Retardation, Autosomal Dominant 7 MNT185
Mental Retardation, Autosomal Recessive 14 MNT154
Mental Retardation, Autosomal Recessive 15 MNT150
Mental Retardation, Autosomal Recessive 16 MNT167
Mental Retardation, Autosomal Recessive 18 MNT151
Mental Retardation, Autosomal Recessive 19 MNT182
Mental Retardation, Autosomal Recessive 2 MNT155
Mental Retardation, Autosomal Recessive 23 MNT170
Mental Retardation, Autosomal Recessive 24 MNT162
Mental Retardation, Autosomal Recessive 25 MNT172
Mental Retardation, Autosomal Recessive 27 MNT177
Mental Retardation, Autosomal Recessive 28 MNT165
Mental Retardation, Autosomal Recessive 29 MNT161
Mental Retardation, Autosomal Recessive 30 MNT163
Mental Retardation, Autosomal Recessive 31 MNT160
Mental Retardation, Autosomal Recessive 33 MNT180
Mental Retardation, Autosomal Recessive 34, with Variant Lissencephaly MNT283
Mental Retardation, Autosomal Recessive 35 MNT181
Mental Retardation, Autosomal Recessive 36 MNT183
Mental Retardation, Autosomal Recessive 37 MNT321
Mental Retardation, Autosomal Recessive 38 MNT176
Mental Retardation, Autosomal Recessive 39 MNT166
Mental Retardation, Autosomal Recessive 40 MNT213
Mental Retardation, Autosomal Recessive 41 MNT216
Mental Retardation, Autosomal Recessive 42 MNT210
Mental Retardation, Autosomal Recessive 43 MNT215
Mental Retardation, Autosomal Recessive 44 MNT221
Mental Retardation, Autosomal Recessive 45 MNT220
Mental Retardation, Autosomal Recessive 46 MNT227
Mental Retardation, Autosomal Recessive 47 MNT225
Mental Retardation, Autosomal Recessive 48 MNT234
Mental Retardation, Autosomal Recessive 49 MNT244
Mental Retardation, Autosomal Recessive 5 MNT145
Mental Retardation, Autosomal Recessive 50 MNT243
Mental Retardation, Autosomal Recessive 51 MNT263
Mental Retardation, Autosomal Recessive 52 MNT264
Mental Retardation, Autosomal Recessive 53 MNT270
Mental Retardation, Autosomal Recessive 54 MNT277
Mental Retardation, Autosomal Recessive 55 MNT282
Mental Retardation, Autosomal Recessive 56 MNT284
Mental Retardation, Autosomal Recessive 57 MNT287
Mental Retardation, Autosomal Recessive 58 MNT285
Mental Retardation, Autosomal Recessive 59 MNT281
Mental Retardation, Autosomal Recessive 60 MNT275
Mental Retardation, Autosomal Recessive 61 MNT325
Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma MNT317
Mental Retardation, Fra12a Type MNT107
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism MNT315
Mental Retardation, Severe, with Spasticity and Pigmentary Tapetoretinal Degeneration MNT311
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy MNT252
Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome MNT318
Mental Retardation, X-Linked 100 MNT223
Mental Retardation, X-Linked 101 MNT224
Mental Retardation, X-Linked 102 MNT248
Mental Retardation, X-Linked 103 MNT289
Mental Retardation, X-Linked 104 MNT267
Mental Retardation, X-Linked 105 MNT274
Mental Retardation, X-Linked 106 MNT294
Mental Retardation, X-Linked 107 MNT333
Mental Retardation, X-Linked 12 MNT305
Mental Retardation, X-Linked 21 MNT301
Mental Retardation, X-Linked 23 MNT204
Mental Retardation, X-Linked 42 MNT205
Mental Retardation, X-Linked 49 MNT187
Mental Retardation, X-Linked 50 MNT194
Mental Retardation, X-Linked 53 MNT202
Mental Retardation, X-Linked 61 MNT271
Mental Retardation, X-Linked 73 MNT247
Mental Retardation, X-Linked 92 MNT196
Mental Retardation, X-Linked 96 MNT195
Mental Retardation, X-Linked 97 MNT200
Mental Retardation, X-Linked 98 MNT198
Mental Retardation, X-Linked 99 MNT218
Mental Retardation, X-Linked 99, Syndromic, Female-Restricted MNT290
Mental Retardation, X-Linked, Associated with Fragile Site Fraxe MNT307
Mental Retardation, X-Linked, Syndromic 13 MNT135
Mental Retardation, X-Linked, Syndromic 17 MNT191
Mental Retardation, X-Linked, Syndromic 32 MNT207
Mental Retardation, X-Linked, Syndromic 33 MNT295
Mental Retardation, X-Linked, Syndromic 34 MNT296
Mental Retardation, X-Linked, Syndromic 9 MNT197
Mental Retardation, X-Linked, Syndromic, 35 MNT298
Mental Retardation, X-Linked, Syndromic, Bain Type MNT269
Mental Retardation, X-Linked, Syndromic, Cabezas Type MNT303
Mental Retardation, X-Linked, Syndromic, Christianson Type MNT302
Mental Retardation, X-Linked, Syndromic, Chudley-Schwartz Type MNT201
Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type MNT228
Mental Retardation, X-Linked, Syndromic, Hedera Type MNT192
Mental Retardation, X-Linked, Syndromic, Houge Type MNT306
Mental Retardation, X-Linked, Syndromic, Martin-Probst Type MNT146
Mental Retardation, X-Linked, Syndromic, Nascimento Type MNT056
Mental Retardation, X-Linked, Syndromic, Raymond Type MNT057
Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type MNT310
Mental Retardation, X-Linked, Syndromic, Turner Type MNT058
Mental Retardation, X-Linked, Syndromic, Wu Type MNT258
Mental Retardation, X-Linked, with Cerebellar Hypoplasia and Distinctive Facial Appearance MNT229
Mental Retardation, X-Linked, with or Without Seizures, Arx-Related MNT304
Mental Retardation, X-Linked, with Panhypopituitarism MNT300
Mercaptolactate-Cysteine Disulfiduria MRC009
Mercury Poisoning MRC003
Merkel Cell Carcinoma MRK001
Mesangial Proliferative Glomerulonephritis MSN001
Mesangioproliferative Glomerulopathy MSN011
Mesenchymal Cell Neoplasm MSN004
Mesenchymal Chondrosarcoma MSN005
Mesenchymoma MSN006
Mesenteric Lymphadenitis MSN002
Mesenteric Vascular Occlusion MSN003
Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis MSL004
Mesocestoidiasis MSC001
Mesomelia MSM003
Mesomelia-Synostoses Syndrome MSM004
Mesomelic Dysplasia, Kantaputra Type MSM016
Mesomelic Dysplasia, Savarirayan Type MSM019
Mesothelioma, Malignant MST023
Metabolic Acidosis MTB004
Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration MTB007
Metacarpal 4-5 Fusion MTC100
Metachondromatosis MTC018
Metachromatic Leukodystrophy MTC003
Metachromatic Leukodystrophy Due to Saposin B Deficiency MTC019
Metachromatic Leukodystrophy, Adult Form MTC074
Metachromatic Leukodystrophy, Juvenile Form MTC076
Metachromatic Leukodystrophy, Late Infantile Form MTC075
Metagonimiasis MTG001
Metal Allergy MTL005
Metal Metabolism Disorder MTL002
Metanephric Adenoma MTN001
Metaphyseal Anadysplasia MTP005
Metaphyseal Anadysplasia 2 MTP014
Metaphyseal Chondrodysplasia, Jansen Type MTP034
Metaphyseal Chondrodysplasia, Schmid Type MTP025
Metaphyseal Dysplasia Maxillary Hypoplasia Brachydactyly MTP010
Metaphyseal Dysplasia with Maxillary Hypoplasia with or Without Brachydactyly MTP023
Metaphyseal Dysplasia Without Hypotrichosis MTP003
Metaphyseal Dysplasia, Spahr Type MTP028
Metaphyseal Enchondromatosis with D-2-Hydroxyglutaric Aciduria MTP033
Metaphyseal Undermodeling, Spondylar Dysplasia, and Overgrowth MTP011
Metatarsus Adductus MTT004
Metatropic Dysplasia MTT002
Metatypical Basal Cell Carcinoma MTT001
Methane Production MTH071
Methanol Poisoning MTH047
Methemoglobin Reductase Deficiency MTH072
Methemoglobinemia MTH007
Methemoglobinemia and Ambiguous Genitalia MTH082
Methemoglobinemia Due to Deficiency of Methemoglobin Reductase MTH026
Methemoglobinemia, Alpha Type MTH084
Methemoglobinemia, Beta Type MTH083
Methemoglobinemia, Beta-Globin Type MTH064
Methionine Adenosyltransferase Deficiency MTH011
Methionine Adenosyltransferase I/iii Deficiency MTH074
Methotrexate Toxicity or Dose Selection MTH061
Methylmalonate Semialdehyde Dehydrogenase Deficiency MTH013
Methylmalonic Acidemia and Homocysteinemia, Cblx Type MTH079
Methylmalonic Acidemia Due to Transcobalamin Receptor Defect MTH069
Methylmalonic Acidemia with Homocystinuria MTH021
Methylmalonic Aciduria and Homocystinuria Type Cble MTH003
Methylmalonic Aciduria and Homocystinuria Type Cblg MTH002
Methylmalonic Aciduria and Homocystinuria, Cblc Type MTH054
Methylmalonic Aciduria and Homocystinuria, Cbld Type MTH055
Methylmalonic Aciduria and Homocystinuria, Cblf Type MTH056
Methylmalonic Aciduria and Homocystinuria, Cblj Type MTH051
Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency MTH076
Methylmalonic Aciduria, Cbla Type MTH077
Methylmalonic Aciduria, Cblb Type MTH078
Methylmalonic Aciduria, Transient, Due to Transcobalamin Receptor Defect MTH068
Methylmalonyl-Coa Epimerase Deficiency MTH040
Methylmalonyl-Coenzyme a Mutase Deficiency MTH025
Metopic Ridging-Ptosis-Facial Dysmorphism Syndrome MTP038
Mevalonic Aciduria MVL001
Microcephalic Osteodysplastic Primordial Dwarfism, Type I MCR240
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii MCR258
Microcephalic Primordial Dwarfism-Insulin Resistance Syndrome MCR279
Microcephaly MCR010
Microcephaly 1, Primary, Autosomal Recessive MCR247
Microcephaly 10, Primary, Autosomal Recessive MCR223
Microcephaly 11, Primary, Autosomal Recessive MCR249
Microcephaly 12, Primary, Autosomal Recessive MCR246
Microcephaly 13, Primary, Autosomal Recessive MCR236
Microcephaly 14, Primary, Autosomal Recessive MCR270
Microcephaly 15, Primary, Autosomal Recessive MCR269
Microcephaly 16, Primary, Autosomal Recessive MCR314
Microcephaly 17, Primary, Autosomal Recessive MCR320
Microcephaly 18, Primary, Autosomal Dominant MCR322
Microcephaly 19, Primary, Autosomal Recessive MCR356
Microcephaly 2, Primary, Autosomal Recessive, with or Without Cortical Malformations MCR222
Microcephaly 20, Primary, Autosomal Recessive MCR360
Microcephaly 21, Primary, Autosomal Recessive MCR361
Microcephaly 22, Primary, Autosomal Recessive MCR362
Microcephaly 23, Primary, Autosomal Recessive MCR363
Microcephaly 3, Primary, Autosomal Recessive MCR248
Microcephaly 4, Primary, Autosomal Recessive MCR254
Microcephaly 5, Primary, Autosomal Recessive MCR239
Microcephaly 6, Primary, Autosomal Recessive MCR250
Microcephaly 7, Primary, Autosomal Recessive MCR238
Microcephaly 8, Primary, Autosomal Recessive MCR243
Microcephaly 9, Primary, Autosomal Recessive MCR255
Microcephaly and Chorioretinopathy, Autosomal Recessive, 1 MCR259
Microcephaly and Chorioretinopathy, Autosomal Recessive, 2 MCR244
Microcephaly and Chorioretinopathy, Autosomal Recessive, 3 MCR272
Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation MCR216
Microcephaly with Simplified Gyral Pattern MCR345
Microcephaly with Spastic Quadriplegia MCR060
Microcephaly-Capillary Malformation Syndrome MCR183
Microcephaly-Complex Motor and Sensory Axonal Neuropathy Syndrome MCR298
Microcephaly-Corpus Callosum and Cerebellar Vermis Hypoplasia-Facial Dysmorphism-Intellectual Disability Syndrom MCR358
Microcephaly-Micromelia Syndrome MCR326
Microcephaly-Polymicrogyria-Corpus Callosum Agenesis Syndrome MCR285
Microcephaly-Short Stature-Intellectual Disability-Facial Dysmorphism Syndrome MCR280
Microcephaly, Amish Type MCR257
Microcephaly, Autosomal Dominant MCR329
Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis MCR315
Microcephaly, Epilepsy, and Diabetes Syndrome MCR209
Microcephaly, Postnatal Progressive, with Seizures and Brain Atrophy MCR123
Microcephaly, Progressive, with Seizures and Cerebral and Cerebellar Atrophy MCR355
Microcephaly, Seizures, and Developmental Delay MCR064
Microcephaly, Seizures, Spasticity, and Brain Calcifications MCR333
Microcephaly, Short Stature, and Impaired Glucose Metabolism 1 MCR323
Microcephaly, Short Stature, and Impaired Glucose Metabolism 2 MCR316
Microcephaly, Short Stature, and Limb Abnormalities MCR327
Microcephaly, Short Stature, and Polymicrogyria with or Without Seizures MCR354
Microcolon MCR334
Microcoria, Congenital MCR067
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus MCR220
Microcystic Adenoma MCR014
Microcystic Meningioma MCR001
Microcytic Anemia MCR018
Microform Holoprosencephaly MCR173
Microglandular Adenosis MCR019
Microhydranencephaly MCR025
Microinvasive Cervical Squamous Cell Carcinoma MCR015
Microinvasive Gastric Cancer MCR011
Microlissencephaly MCR099
Microphthalmia MCR013
Microphthalmia with Limb Anomalies MCR165
Microphthalmia, Isolated 1 MCR124
Microphthalmia, Isolated 2 MCR137
Microphthalmia, Isolated 3 MCR114
Microphthalmia, Isolated 4 MCR109
Microphthalmia, Isolated 5 MCR122
Microphthalmia, Isolated 6 MCR211
Microphthalmia, Isolated 7 MCR108
Microphthalmia, Isolated 8 MCR219
Microphthalmia, Isolated, with Cataract 1 MCR330
Microphthalmia, Isolated, with Coloboma 1 MCR338
Microphthalmia, Isolated, with Coloboma 10 MCR271
Microphthalmia, Isolated, with Coloboma 2 MCR346
Microphthalmia, Isolated, with Coloboma 3 MCR349
Microphthalmia, Isolated, with Coloboma 5 MCR350
Microphthalmia, Isolated, with Coloboma 6 MCR352
Microphthalmia, Isolated, with Coloboma 7 MCR210
Microphthalmia, Isolated, with Coloboma 9 MCR214
Microphthalmia, Syndromic 1 MCR263
Microphthalmia, Syndromic 11 MCR217
Microphthalmia, Syndromic 12 MCR212
Microphthalmia, Syndromic 13 MCR228
Microphthalmia, Syndromic 2 MCR261
Microphthalmia, Syndromic 3 MCR241
Microphthalmia, Syndromic 4 MCR262
Microphthalmia, Syndromic 5 MCR252
Microphthalmia, Syndromic 6 MCR251
Microphthalmia, Syndromic 8 MCR245
Microphthalmia, Syndromic 9 MCR256
Microphthalmia/coloboma and Skeletal Dysplasia Syndrome MCR324
Microscopic Colitis MCR191
Microscopic Polyangiitis MCR088
Microspherophakia and/or Megalocornea, with Ectopia Lentis and with or Without Secondary Glaucoma MCR253
Microsporidiosis MCR020
Microtia MCR103
Microtia with Nasolacrimal Duct Imperforation and Eye Coloboma MCR242
Microtia, Hearing Impairment, and Cleft Palate MCR119
Microvascular Complications of Diabetes 1 MCR129
Microvascular Complications of Diabetes 2 MCR112
Microvascular Complications of Diabetes 3 MCR113
Microvascular Complications of Diabetes 4 MCR133
Microvascular Complications of Diabetes 5 MCR115
Microvascular Complications of Diabetes 6 MCR130
Microvascular Complications of Diabetes 7 MCR120
Mid-Dermal Elastolysis MDD015
Middle Cerebral Artery Infarction MDD003
Middle Cranial Fossa Meningioma MDD001
Middle Ear Adenoma MDD008
Middle Ear Carcinoma MDD009
Middle Ear Cholesterol Granuloma MDD006
Middle Ear Disease MDD010
Middle Ear Squamous Cell Carcinoma MDD007
Middle Lobe Syndrome MDD005
Midface Hypoplasia, Hearing Impairment, Elliptocytosis, and Nephrocalcinosis MDF002
Midline Interhemispheric Variant of Holoprosencephaly MDL020
Migraine with Aura MGR003
Migraine with Aura 7 MGR025
Migraine with Aura 9 MGR027
Migraine with Brainstem Aura MGR035
Migraine with or Without Aura 1 MGR028
Migraine with or Without Aura 12 MGR040
Migraine with or Without Aura 13 MGR042
Migraine with or Without Aura 2 MGR036
Migraine with or Without Aura 3 MGR022
Migraine with or Without Aura 5 MGR024
Migraine with or Without Aura 6 MGR033
Migraine with or Without Aura 8 MGR037
Migraine Without Aura MGR001
Migraine Without Aura 4 MGR023
Migraine, Familial Hemiplegic, 1 MGR032
Migraine, Familial Hemiplegic, 2 MGR030
Migraine, Familial Hemiplegic, 3 MGR031
Mikulicz Disease MKL001
Mild Hemophilia a MLD013
Mild Hyperphenylalaninemia MLD011
Mild Phenylketonuria MLD010
Mild Pre-Eclampsia MLD002
Miles-Carpenter Syndrome MLS013
Miliaria MLR009
Miliaria Rubra MLR001
Miliary Tuberculosis MLR002
Milk Allergy MLK006
Milker's Nodule MLK001
Miller Fisher Syndrome MLL002
Miller-Dieker Lissencephaly Syndrome MLL018
Mineral Metabolism Disease MNR003
Minicore Myopathy with External Ophthalmoplegia MNC011
Minimal Pigment Oculocutaneous Albinism Type 1 MNM005
Mirage Syndrome MRG013
Mirror Movements 1 MRR011
Mirror Movements 2 MRR010
Mirror Movements 3 MRR012
Mismatch Repair Cancer Syndrome MSM014
Mitchell-Riley Syndrome MTC096
Mite Infestation MTN002
Mitochondrial Complex I Deficiency MTC007
Mitochondrial Complex I Deficiency Due to Acad9 Deficiency MTC107
Mitochondrial Complex Ii Deficiency MTC020
Mitochondrial Complex Iii Deficiency MTC008
Mitochondrial Complex Iii Deficiency, Nuclear Type 1 MTC085 MC3DN1
Mitochondrial Complex Iii Deficiency, Nuclear Type 2 MTC091
Mitochondrial Complex Iii Deficiency, Nuclear Type 3 MTC089
Mitochondrial Complex Iii Deficiency, Nuclear Type 4 MTC087
Mitochondrial Complex Iii Deficiency, Nuclear Type 6 MTC090
Mitochondrial Complex Iii Deficiency, Nuclear Type 7 MTC095
Mitochondrial Complex Iii Deficiency, Nuclear Type 8 MTC094
Mitochondrial Complex Iii Deficiency, Nuclear Type 9 MTC098
Mitochondrial Complex Iv Deficiency MTC097
Mitochondrial Complex V Deficiency MTC021
Mitochondrial Complex V Deficiency, Nuclear Type 1 MTC029
Mitochondrial Complex V Deficiency, Nuclear Type 2 MTC068
Mitochondrial Complex V Deficiency, Nuclear Type 3 MTC030
Mitochondrial Complex V Deficiency, Nuclear Type 4 MTC137
Mitochondrial Disorders MTC069
Mitochondrial Dna Depletion Syndrome 1 MTC061
Mitochondrial Dna Depletion Syndrome 11 MTC078
Mitochondrial Dna Depletion Syndrome 12a , Autosomal Dominant MTC139
Mitochondrial Dna Depletion Syndrome 12b , Autosomal Recessive MTC138
Mitochondrial Dna Depletion Syndrome 13 MTC088
Mitochondrial Dna Depletion Syndrome 14 MTC126
Mitochondrial Dna Depletion Syndrome 15 MTC129
Mitochondrial Dna Depletion Syndrome 2 MTC062
Mitochondrial Dna Depletion Syndrome 3 MTC063
Mitochondrial Dna Depletion Syndrome 4a MTC056
Mitochondrial Dna Depletion Syndrome 4b MTC055
Mitochondrial Dna Depletion Syndrome 5 MTC059
Mitochondrial Dna Depletion Syndrome 6 MTC058
Mitochondrial Dna Depletion Syndrome 7 MTC054
Mitochondrial Dna Depletion Syndrome 8a MTC065
Mitochondrial Dna Depletion Syndrome 9 MTC060
Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form MTC093
Mitochondrial Dna-Associated Leigh Syndrome and Narp MTC015
Mitochondrial Encephalomyopathy MTC004
Mitochondrial Membrane Protein-Associated Neurodegeneration MTC036
Mitochondrial Metabolism Disease MTC005
Mitochondrial Myopathy MTC133
Mitochondrial Myopathy with Diabetes MTC025
Mitochondrial Myopathy with Lactic Acidosis MTC026
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes MTC114
Mitochondrial Myopathy, Infantile, Transient MTC116
Mitochondrial Myopathy, Lethal, Infantile MTC115
Mitochondrial Neurogastrointestinal Encephalomyopathy MTC111
Mitochondrial Neurogastrointestinal Encephalopathy Disease MTC016
Mitochondrial Non-Syndromic Sensorineural Deafness MTC106
Mitochondrial Phosphate Carrier Deficiency MTC037
Mitochondrial Pyruvate Carrier Deficiency MTC079
Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency MTC108
Mitochondrial Trifunctional Protein Deficiency MTC027
Mitral Atresia MTR027
Mitral Valve Disease MTR012
Mitral Valve Insufficiency MTR002
Mitral Valve Prolapse 1 MTR080
Mitral Valve Prolapse 2 MTR077
Mitral Valve Prolapse 3 MTR083
Mitral Valve Stenosis MTR003
Mixed Astrocytoma-Ependymoma MXD011
Mixed Cell Adenoma MXD020
Mixed Cell Type Cancer MXD023
Mixed Cerebral Palsy MXD001
Mixed Connective Tissue Disease MXD005
Mixed Ductal-Endocrine Carcinoma MXD014
Mixed Endometrial Stromal and Smooth Muscle Tumor MXD017
Mixed Fibrolamellar Hepatocellular Carcinoma MXD042
Mixed Germ Cell Cancer MXD025
Mixed Germ Cell Tumor MXD032
Mixed Glioma MXD026
Mixed Gonadal Dysgenesis MXD016
Mixed Hepatoblastoma MXD007
Mixed Lacrimal Gland Cancer MXD003
Mixed Liposarcoma MXD006
Mixed Malaria MXD019
Mixed Oligodendroglioma-Astrocytoma MXD012
Mixed Type Thymoma MXD027
Miyoshi Muscular Dystrophy 1 MYS033
Miyoshi Muscular Dystrophy 2 MYS019
Miyoshi Muscular Dystrophy 3 MYS014
Mn1 MN1001
Moderate and Severe Traumatic Brain Injury MDR006
Moderately Severe Hemophilia a MDR007
Moebius Syndrome MBS002
Mohr Syndrome MHR002
Mohr-Tranebjaerg Syndrome MHR001
Molluscum Contagiosum MLL001
Molybdenum Cofactor Deficiency MLY001
Molybdenum Cofactor Deficiency, Complementation Group a MLY008
Molybdenum Cofactor Deficiency, Complementation Group B MLY009
Molybdenum Cofactor Deficiency, Complementation Group C MLY010
Momo Syndrome MMS001
Mondini Dysplasia MND005
Mongolian Spot MNG001
Monilethrix MNL001
Monkeypox MNK002
Monocarboxylate Transporter 1 Deficiency MNC019
Monoclonal Gammopathy of Uncertain Significance MNC006
Monoclonal Paraproteinemia MNC004
Monocytic Leukemia MNC007
Monofixation Syndrome MNF001
Monogenic Diabetes MNG006
Mononeuritis Multiplex MNN002
Mononeuritis of Lower Limb MNN015
Mononeuritis of Upper Limb and Mononeuritis Multiplex MNN016
Mononeuropathy MNN017
Mononeuropathy of the Median Nerve, Mild MNN028
Monophasic Synovial Sarcoma MNP001
Monosomy 21 MNS008
Monosomy 22 MNS014
Monosomy 7 of Bone Marrow MNS016
Monosomy 9q22.3 MNS011
Monostotic Fibrous Dysplasia MNS012
Mood Disorder MDD011
Mooren's Ulcer MRN002
Morbid Obesity MRB003
Morbid Obesity and Spermatogenic Failure MRB006
Morgagni Cataract MRG001
Morning Glory Syndrome MRN009
Morpheaform Basal Cell Carcinoma MRP002
Morphine Dependence MRP001
Morquio Syndrome MRQ003
Morvan's Fibrillary Chorea MRV001
Mosaic Trisomy 8 MSC020
Mosaic Variegated Aneuploidy Syndrome MSC022
Mosaic Variegated Aneuploidy Syndrome 1 MSC109
Mosaic Variegated Aneuploidy Syndrome 2 MSC106
Mosaic Variegated Aneuploidy Syndrome 3 MSC139
Motion Sickness MTN003
Motor Neuron Disease MTR014
Motor Peripheral Neuropathy MTR007
Mouth Disease MTH009
Movement Disease MVM001
Mowat-Wilson Syndrome MWT001
Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation MWT004
Mowat-Wilson Syndrome Due to Monosomy 2q22 MWT002
Moyamoya Disease 1 MYM013
Moyamoya Disease 2 MYM004
Moyamoya Disease 3 MYM005
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism MYM012
Moyamoya Disease 5 MYM003
Moyamoya Disease 6 with Achalasia MYM014
Mthfr Gene Variant MTH081
Mu Chain Disease MCH003
Mucin-1 Kidney Disease MCN024
Mucinoses MCN011
Mucinous Adenocarcinoma MCN001
Mucinous Adenocarcinoma of the Appendix MCN018
Mucinous Adenofibroma MCN006
Mucinous Bronchioloalveolar Adenocarcinoma MCN021
Mucinous Cystadenocarcinoma MCN008
Mucinous Cystadenocarcinoma of the Pancreas MCN022
Mucinous Cystadenofibroma MCN010
Mucinous Intrahepatic Cholangiocarcinoma MCN005
Mucinous Lung Adenocarcinoma MCN023
Mucinous Ovarian Cystadenoma MCN003
Mucinous Stomach Adenocarcinoma MCN009
Mucinous Tubular and Spindle Renal Cell Carcinoma MCN004
Muckle-Wells Syndrome MCK007
Mucocele of Appendix MCC004
Mucocele of Salivary Gland MCC003
Mucocutaneous Leishmaniasis MCC002
Mucoepidermoid Carcinoma MCP006
Mucoepidermoid Esophageal Carcinoma MCP008
Mucoepidermoid Thyroid Carcinoma MCP007
Mucolipidoses MCL022
Mucolipidosis Ii Alpha/beta MCL062
Mucolipidosis Iii Alpha/beta MCL046
Mucolipidosis Iii Gamma MCL016
Mucolipidosis Iv MCL013
Mucopolysaccharidoses MCP033
Mucopolysaccharidosis Iii MCP001
Mucopolysaccharidosis Iv MCP004
Mucopolysaccharidosis Type 2, Attenuated Form MCP034
Mucopolysaccharidosis Type 2, Severe Form MCP035
Mucopolysaccharidosis Type 6, Rapidly Progressing MCP029
Mucopolysaccharidosis Type 6, Slowly Progressing MCP028
Mucopolysaccharidosis Type Vi MCP024
Mucopolysaccharidosis-Plus Syndrome MCP040
Mucopolysaccharidosis, Type Ii MCP050
Mucopolysaccharidosis, Type Iiia MCP043
Mucopolysaccharidosis, Type Iiib MCP044
Mucopolysaccharidosis, Type Iiic MCP045
Mucopolysaccharidosis, Type Iiid MCP046
Mucopolysaccharidosis, Type Iva MCP047
Mucopolysaccharidosis, Type Ivb MCP048
Mucopolysaccharidosis, Type Ix MCP051
Mucopolysaccharidosis, Type Vii MCP049
Mucosal Melanoma MCS004
Mucositis MCS002
Muenke Syndrome MNK003
Muir-Torre Syndrome MRT001
Mulchandani-Bhoj-Conlin Syndrome MLC004
Mulibrey Nanism MLB001
Mullerian Aplasia MLL009
Mullerian Aplasia and Hyperandrogenism MLL011
Multicentric Carpotarsal Osteolysis Syndrome MLT092
Multicentric Castleman Disease MLT113
Multicentric Osteolysis Nephropathy MLT033
Multicentric Osteolysis, Nodulosis, and Arthropathy MLT065
Multicentric Papillary Thyroid Carcinoma MLT005
Multicentric Reticulohistiocytosis MLT016
Multicystic Dysplastic Kidney MLT084
Multidrug-Resistant Tuberculosis MLT006
Multifocal Choroiditis MLT035
Multifocal Dystonia MLT132
Multifocal Motor Neuropathy MLT075
Multifocal Osteogenic Sarcoma MLT017
Multifocal Pattern Dystrophy Simulating Fundus Flavimaculatus MLT117
Multilocular Clear Cell Renal Cell Carcinoma MLT003
Multiminicore Disease MLT028
Multinodular Goiter MLT008
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly MLT161
Multiple Acyl-Coa Dehydrogenase Deficiency MLT118
Multiple Benign Circumferential Skin Creases on Limbs MLT104
Multiple Carboxylase Deficiency MLT018
Multiple Chemical Sensitivity MLT001
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome MLT140
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1 MLT126
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 MLT128
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 MLT127
Multiple Cranial Nerve Palsy MLT009
Multiple Enchondromatosis, Maffucci Type MLT145
Multiple Endocrine Neoplasia MLT074
Multiple Endocrine Neoplasia, Type I MLT156
Multiple Endocrine Neoplasia, Type Iia MLT160
Multiple Endocrine Neoplasia, Type Iib MLT159
Multiple Endocrine Neoplasia, Type Iv MLT086
Multiple Epiphyseal Dysplasia MLT007
Multiple Epiphyseal Dysplasia Due to Collagen 9 Anomaly MLT141
Multiple Familial Trichoepithelioma MLT048
Multiple Fibroadenomas of the Breast MLT120
Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects MLT162
Multiple Mitochondrial Dysfunctions Syndrome MLT027
Multiple Mitochondrial Dysfunctions Syndrome 1 MLT068
Multiple Mitochondrial Dysfunctions Syndrome 2 MLT069
Multiple Mitochondrial Dysfunctions Syndrome 2 with Hyperglycinemia MLT150
Multiple Mitochondrial Dysfunctions Syndrome 3 MLT119
Multiple Mitochondrial Dysfunctions Syndrome 4 MLT139
Multiple Mitochondrial Dysfunctions Syndrome 5 MLT151
Multiple Mitochondrial Dysfunctions Syndrome 6 MLT167
Multiple Mucosal Neuroma MLT011
Multiple Paragangliomas Associated with Polycythemia MLT106
Multiple Personality Disorder MLT010
Multiple Pterygium Syndrome, Escobar Variant MLT163
Multiple Pterygium Syndrome, Lethal Type MLT134
Multiple Sclerosis MLT020 MS
Multiple Sclerosis 2 MLT093
Multiple Sclerosis 3 MLT094
Multiple Sclerosis 4 MLT095
Multiple Sclerosis 5 MLT124
Multiple Self-Healing Squamous Epithelioma MLT152
Multiple Sulfatase Deficiency MLT135
Multiple Synostoses Syndrome MLT072
Multiple Synostoses Syndrome 1 MLT059
Multiple Synostoses Syndrome 2 MLT060
Multiple Synostoses Syndrome 3 MLT078
Multiple Synostoses Syndrome 4 MLT166
Multiple System Atrophy 1 MLT157
Multiple System Atrophy, Cerebellar Type MLT105
Multiple System Atrophy, Parkinsonian Type MLT116
Multisystemic Smooth Muscle Dysfunction Syndrome MLT073
Mumps MMP001
Munchausen by Proxy MNC002
Mungan Syndrome MNG003
Murcs Association MRC004
Murray Valley Encephalitis MRR003
Muscle Cancer MSC072
Muscle Disorders MSC033
Muscle Eye Brain Disease MSC077
Muscle Hypertrophy MSC007
Muscle Strength Quantitative Trait Locus 1 MSC054
Muscle Tissue Disease MSC004
Muscular Atrophy MSC003
Muscular Dystrophy MSC005
Muscular Dystrophy-Dystroglycanopathy MSC002
Muscular Dystrophy-Dystroglycanopathy , Type a, 1 MSC047
Muscular Dystrophy-Dystroglycanopathy , Type a, 10 MSC107
Muscular Dystrophy-Dystroglycanopathy , Type a, 11 MSC167
Muscular Dystrophy-Dystroglycanopathy , Type a, 12 MSC102
Muscular Dystrophy-Dystroglycanopathy , Type a, 13 MSC105
Muscular Dystrophy-Dystroglycanopathy , Type a, 14 MSC097
Muscular Dystrophy-Dystroglycanopathy , Type a, 2 MSC043
Muscular Dystrophy-Dystroglycanopathy , Type a, 3 MSC045
Muscular Dystrophy-Dystroglycanopathy , Type a, 4 MSC037
Muscular Dystrophy-Dystroglycanopathy , Type a, 5 MSC034
Muscular Dystrophy-Dystroglycanopathy , Type a, 6 MSC041
Muscular Dystrophy-Dystroglycanopathy , Type a, 7 MSC101
Muscular Dystrophy-Dystroglycanopathy , Type a, 8 MSC166
Muscular Dystrophy-Dystroglycanopathy , Type a, 9 MSC127
Muscular Dystrophy-Dystroglycanopathy , Type B, 1 MSC048
Muscular Dystrophy-Dystroglycanopathy , Type B, 14 MSC099
Muscular Dystrophy-Dystroglycanopathy , Type B, 2 MSC044
Muscular Dystrophy-Dystroglycanopathy , Type B, 3 MSC046
Muscular Dystrophy-Dystroglycanopathy , Type B, 4 MSC038
Muscular Dystrophy-Dystroglycanopathy , Type B, 5 MSC035
Muscular Dystrophy-Dystroglycanopathy , Type B, 6 MSC042
Muscular Dystrophy-Dystroglycanopathy , Type C, 1 MSC104
Muscular Dystrophy-Dystroglycanopathy , Type C, 12 MSC118
Muscular Dystrophy-Dystroglycanopathy , Type C, 14 MSC098
Muscular Dystrophy-Dystroglycanopathy , Type C, 2 MSC108
Muscular Dystrophy-Dystroglycanopathy , Type C, 3 MSC093
Muscular Dystrophy-Dystroglycanopathy , Type C, 4 MSC103
Muscular Dystrophy-Dystroglycanopathy , Type C, 5 MSC036
Muscular Dystrophy-Dystroglycanopathy , Type C, 7 MSC111
Muscular Dystrophy-Dystroglycanopathy , Type C, 9 MSC100
Muscular Dystrophy, Becker Type MSC152
Muscular Dystrophy, Congenital Merosin-Deficient, 1a MSC162
Muscular Dystrophy, Congenital, 1b MSC050
Muscular Dystrophy, Congenital, Davignon-Chauveau Type MSC141
Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency MSC164
Muscular Dystrophy, Congenital, Lmna-Related MSC165
Muscular Dystrophy, Congenital, Megaconial Type MSC028
Muscular Dystrophy, Congenital, Merosin-Positive MSC029
Muscular Dystrophy, Congenital, with Cataracts and Intellectual Disability MSC142
Muscular Dystrophy, Duchenne Type MSC157
Muscular Dystrophy, Limb-Girdle, Type 1a MSC115
Muscular Dystrophy, Limb-Girdle, Type 1b MSC112
Muscular Dystrophy, Limb-Girdle, Type 1c MSC161
Muscular Dystrophy, Limb-Girdle, Type 1e MSC117
Muscular Dystrophy, Limb-Girdle, Type 1f MSC057
Muscular Dystrophy, Limb-Girdle, Type 1h MSC058
Muscular Dystrophy, Limb-Girdle, Type 2a MSC121
Muscular Dystrophy, Limb-Girdle, Type 2b MSC113
Muscular Dystrophy, Limb-Girdle, Type 2c MSC120
Muscular Dystrophy, Limb-Girdle, Type 2d MSC123
Muscular Dystrophy, Limb-Girdle, Type 2f MSC116
Muscular Dystrophy, Limb-Girdle, Type 2g MSC122
Muscular Dystrophy, Limb-Girdle, Type 2h MSC119
Muscular Dystrophy, Limb-Girdle, Type 2j MSC063
Muscular Dystrophy, Limb-Girdle, Type 2l MSC059
Muscular Dystrophy, Limb-Girdle, Type 2q MSC062
Muscular Dystrophy, Limb-Girdle, Type 2r MSC095
Muscular Dystrophy, Limb-Girdle, Type 2w MSC136
Muscular Dystrophy, Limb-Girdle, Type 2x MSC140
Muscular Dystrophy, Limb-Girdle, Type 2z MSC137
Muscular Phosphorylase Kinase Deficiency MSC031
Musculocontractural Ehlers-Danlos Syndrome MSC134
Musical Aptitude Quantitative Trait Locus MSC163
Mutagen Sensitivity MTG002
Mutism MTS001
Mutyh-Associated Polyposis MTY001
Myasthenia Gravis MYS003
Myasthenia Gravis with Thymus Hyperplasia MYS007
Myasthenic Syndrome, Congenital, 10 MYS052
Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency MYS057
Myasthenic Syndrome, Congenital, 12 MYS074
Myasthenic Syndrome, Congenital, 13 MYS075
Myasthenic Syndrome, Congenital, 14 MYS078
Myasthenic Syndrome, Congenital, 15 MYS077
Myasthenic Syndrome, Congenital, 16 MYS064
Myasthenic Syndrome, Congenital, 17 MYS056
Myasthenic Syndrome, Congenital, 18 MYS065
Myasthenic Syndrome, Congenital, 19 MYS070
Myasthenic Syndrome, Congenital, 1a, Slow-Channel MYS046
Myasthenic Syndrome, Congenital, 1b, Fast-Channel MYS047
Myasthenic Syndrome, Congenital, 20, Presynaptic MYS068
Myasthenic Syndrome, Congenital, 21, Presynaptic MYS069
Myasthenic Syndrome, Congenital, 22 MYS067
Myasthenic Syndrome, Congenital, 2a, Slow-Channel MYS062
Myasthenic Syndrome, Congenital, 2c, Associated with Acetylcholine Receptor Deficiency MYS063
Myasthenic Syndrome, Congenital, 3a, Slow-Channel MYS048
Myasthenic Syndrome, Congenital, 3b, Fast-Channel MYS049
Myasthenic Syndrome, Congenital, 3c, Associated with Acetylcholine Receptor Deficiency MYS050
Myasthenic Syndrome, Congenital, 4a, Slow-Channel MYS059
Myasthenic Syndrome, Congenital, 4b, Fast-Channel MYS060
Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency MYS061
Myasthenic Syndrome, Congenital, 5 MYS051
Myasthenic Syndrome, Congenital, 6, Presynaptic MYS055
Myasthenic Syndrome, Congenital, 7, Presynaptic MYS044
Myasthenic Syndrome, Congenital, 8 MYS076
Myasthenic Syndrome, Congenital, 9, Associated with Acetylcholine Receptor Deficiency MYS054
Mybpc1-Related Autosomal Recessive Non-Lethal Arthrogryposis Multiplex Congenita Syndrome MYB004
Mycetoma MYC012
Mycobacterium Abscessus MYC013
Mycobacterium Chelonae MYC014
Mycobacterium Fortuitum MYC015
Mycobacterium Gordonae MYC016
Mycobacterium Kansasii MYC017
Mycobacterium Malmoense MYC018
Mycobacterium Marinum MYC019
Mycobacterium Tuberculosis 1 MYC084
Mycobacterium Tuberculosis 2 MYC054
Mycobacterium Tuberculosis 3 MYC055
Mycobacterium Tuberculosis X-Linked MYC081
Mycobacterium Tuberculosis, Susceptibility to Infection by MYC020
Mycoplasmal Pneumonia MYC022
Mycosis Fungoides MYC006
Myd88 Deficiency MYD002
Myelitis MYL001
Myelocystocele MYL044
Myelodysplastic Myeloproliferative Cancer MYL004
Myelodysplastic Syndrome MYL009
Myelofibrosis MYL005
Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 MYL059
Myeloid Leukemia MYL006
Myeloid Neoplasms Associated with Pdgfrb Rearrangement MYL061
Myeloid Sarcoma MYL003
Myeloid/lymphoid Neoplasm Associated with Pdgfra Rearrangement MYL066
Myeloid/lymphoid Neoplasm Associated with Pdgfrb Rearrangement MYL065
Myeloma, Multiple MYL069
Myelomeningocele MYL020
Myelopathy, Htlv-1-Associated MYL057
Myeloperoxidase Deficiency MYL013
Myelophthisic Anemia MYL002
Myeloproliferative Disorder, Chronic, with Eosinophilia MYL067
Myeloproliferative Neoplasm MYL031
Myeloproliferative Syndrome, Transient MYL058
Myeloproliferative/lymphoproliferative Neoplasms, Familial MYL064
Myh-9 Related Disease MYH015
Myh9 Related Thrombocytopenia MYH004
Myhre Syndrome MYH012
Myiasis MYS004
Myo5b-Related Progressive Familial Intrahepatic Cholestasis MY5001
Myoblastoma MYB001
Myocardial Infarction MYC007
Myocardial Infarction 2 MYC058
Myocardial Stunning MYC005
Myocarditis MYC008
Myoclonic Astatic Epilepsy MYC023
Myoclonic Cerebellar Dyssynergia MYC001
Myoclonic Epilepsy Associated with Ragged-Red Fibers MYC072
Myoclonic Epilepsy Myopathy Sensory Ataxia MYC030
Myoclonic Epilepsy of Infancy MYC068
Myoclonic Epilepsy of Lafora MYC079
Myoclonic Epilepsy of Unverricht and Lundborg MYC080
Myoclonic Epilepsy, Familial Infantile MYC083
Myoclonic Epilepsy, Juvenile 3 MYC085
Myoclonic Epilepsy, Juvenile 4 MYC086
Myoclonic-Astastic Epilepsy MYC069
Myoclonic-Atonic Epilepsy MYC071
Myoclonus MYC033
Myoclonus and Ataxia MYC078
Myoclonus Epilepsy MYC026
Myoclonus, Familial Cortical MYC066
Myoclonus, Intractable, Neonatal MYC075
Myoepithelioma MYP001
Myofascial Pain Syndrome MYF002
Myofibrillar Myopathy MYF003
Myofibroma MYF001
Myofibromatosis, Infantile, 1 MYF007
Myofibromatosis, Infantile, 2 MYF010
Myoglobinuria MYG005
Myoglobinuria, Acute Recurrent, Autosomal Recessive MYG004
Myoglobinuria, Recurrent MYG007
Myoma MYM001
Myopathic Intestinal Pseudoobstruction MYP066
Myopathy MYP004
Myopathy Due to Myoadenylate Deaminase Deficiency MYP071
Myopathy of Extraocular Muscle MYP005
Myopathy with Extrapyramidal Signs MYP086
Myopathy with Lactic Acidosis, Hereditary MYP097
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset MYP093
Myopathy, Centronuclear, 1 MYP123
Myopathy, Centronuclear, 2 MYP131
Myopathy, Centronuclear, 3 MYP096
Myopathy, Centronuclear, 4 MYP098
Myopathy, Centronuclear, 5 MYP148
Myopathy, Centronuclear, 6, with Fiber-Type Disproportion MYP150
Myopathy, Centronuclear, X-Linked MYP136
Myopathy, Congenital MYP132
Myopathy, Congenital, Compton-North MYP038
Myopathy, Congenital, with Fiber-Type Disproportion MYP091
Myopathy, Congenital, with Fiber-Type Disproportion, X-Linked MYP039
Myopathy, Congenital, with Neuropathy and Deafness MYP122
Myopathy, Distal, 1 MYP125
Myopathy, Distal, 3 MYP112
Myopathy, Distal, 4 MYP095
Myopathy, Distal, 5 MYP116
Myopathy, Distal, Tateyama Type MYP067
Myopathy, Distal, with Anterior Tibial Onset MYP035
Myopathy, Distal, with Rimmed Vacuoles MYP120
Myopathy, Isolated Mitochondrial, Autosomal Dominant MYP099
Myopathy, Lactic Acidosis, and Sideroblastic Anemia MYP108
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1 MYP021
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2 MYP022
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3 MYP107
Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay MYP017
Myopathy, Mitochondrial, and Ataxia MYP149
Myopathy, Myofibrillar, 1 MYP072
Myopathy, Myofibrillar, 2 MYP082
Myopathy, Myofibrillar, 3 MYP078
Myopathy, Myofibrillar, 4 MYP080
Myopathy, Myofibrillar, 5 MYP079
Myopathy, Myofibrillar, 6 MYP081
Myopathy, Myofibrillar, 7 MYP119
Myopathy, Myofibrillar, 8 MYP118
Myopathy, Myofibrillar, Fatal Infantile Hypertonic, Alpha-B Crystallin-Related MYP121
Myopathy, Myosin Storage, Autosomal Dominant MYP105
Myopathy, Myosin Storage, Autosomal Recessive MYP106
Myopathy, Proximal, and Ophthalmoplegia MYP139
Myopathy, Scapulohumeroperoneal MYP114
Myopathy, Spheroid Body MYP094
Myopathy, Tubular Aggregate, 1 MYP087
Myopathy, Tubular Aggregate, 2 MYP088
Myopathy, Vacuolar, with Casq1 Aggregates MYP104
Myopathy, X-Linked, with Excessive Autophagy MYP100
Myopathy, X-Linked, with Postural Muscle Atrophy MYP056
Myopericytoma MYP064
Myopia MYP006
Myopia 1, X-Linked MYP137
Myopia 10 MYP044
Myopia 11, Autosomal Dominant MYP143
Myopia 12, Autosomal Dominant MYP144
Myopia 13, X-Linked MYP134
Myopia 14 MYP069
Myopia 15, Autosomal Dominant MYP146
Myopia 16, Autosomal Dominant MYP145
Myopia 17, Autosomal Dominant MYP140
Myopia 18, Autosomal Recessive MYP133
Myopia 19, Autosomal Dominant MYP147
Myopia 2, Autosomal Dominant MYP127
Myopia 20, Autosomal Dominant MYP084
Myopia 21, Autosomal Dominant MYP070
Myopia 22, Autosomal Dominant MYP075
Myopia 23, Autosomal Recessive MYP074
Myopia 24, Autosomal Dominant MYP090
Myopia 25, Autosomal Dominant MYP117
Myopia 26, X-Linked, Female-Limited MYP135
Myopia 3, Autosomal Dominant MYP138
Myopia 5, Autosomal Dominant MYP141
Myopia 6 MYP018
Myopia 7 MYP040
Myopia 8 MYP041
Myopia 9 MYP048
Myopia, High, with Cataract and Vitreoretinal Degeneration MYP073
Myosclerosis, Autosomal Recessive MYS016
Myosin Storage Myopathy MYS032
Myositis MYS005
Myositis Fibrosa MYS002
Myositis Ossificans MYS001
Myostatin-Related Muscle Hypertrophy MYS010
Myotonia MYT011
Myotonia Congenita MYT023
Myotonia Congenita, Autosomal Dominant MYT027
Myotonia Congenita, Autosomal Recessive MYT029
Myotonia, Potassium-Aggravated MYT030
Myotonic Disease MYT003
Myotonic Dystrophy MYT002
Myotonic Dystrophy 1 MYT021
Myotonic Dystrophy 2 MYT020
Myotubular Myopathy with Abnormal Genital Development MYT025
Myringitis Bullosa Hemorrhagica MYR001
Myxedema MYX004
Myxofibrosarcoma MYX013
Myxoid Chondrosarcoma MYX008
Myxoid Leiomyosarcoma MYX006
Myxoid Liposarcoma MYX005
Myxoid Liposarcoma of the Ovary MYX002
Myxoma, Intracardiac MYX012
Myxopapillary Ependymoma MYX001
Myxosarcoma MYX007
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