Disease Name Symbol Acronym
Machado-Joseph Disease MCH002
Machado-Joseph Disease Type 1 MCH012
Machado-Joseph Disease Type 2 MCH014
Machado-Joseph Disease Type 3 MCH013
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis MCR095
Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation MCR321
Macrocephaly, Macrosomia, Facial Dysmorphism Syndrome MCR221
Macrocephaly/autism Syndrome MCR096
Macrocephaly/megalencephaly Syndrome, Autosomal Recessive MCR237
Macrocytic Anemia MCR017
Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic MCR128
Macrodactyly of Fingers, Unilateral MCR188
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 Progressive Sensorineural Deafness MCR139
Macrothrombocytopenia-Lymphedema-Developmental Delay-Facial Dysmorphism-Camptodactyly Syndrome MCR328
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related MCR125
Macrozoospermia MCR265
Macular Amyloidosis MCL047
Macular Corneal Dystrophy MCL002
Macular Degeneration, Age-Related 5 MCL064
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, Reduced Risk of MCL054
Macular Degeneration, Age-Related, 15 MCL065
Macular Degeneration, Age-Related, 2 MCL043
Macular Degeneration, Age-Related, 4 MCL038
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, Dominant Cystoid MCL027
Macular Dystrophy, North Carolina Type MCL072
Macular Dystrophy, Patterned, 1 MCL059
Macular Dystrophy, Patterned, 2 MCL071
Macular Dystrophy, Patterned, 3 MCL070
Macular Dystrophy, Retinal, 2 MCL035
Macular Dystrophy, Retinal, 3 MCL026
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
Madelung Deformity MDL024
Madras Motor Neuron Disease MDR004
Magi2-Related Infantile Spasms MG2001
Main Bronchus Cancer MNB001
Majeed Syndrome MJD001
Major Affective Disorder 1 MJR007
Major Affective Disorder 2 MJR008
Major Affective Disorder 4 MJR004
Major Affective Disorder 5 MJR006
Major Affective Disorder 6 MJR003
Major Affective Disorder-7 MJR018
Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment MJR011
Mak-Related Retinitis Pigmentosa MKR001
Malaria MLR004
Malaria, Mild MLR020
Male Infertility MLN007
Male Reproductive Organ Benign Neoplasm MLR005
Male Reproductive Organ Cancer MLR006
Male Reproductive System Disease MLR007
Maligant Granulosa Cell Tumor of Ovary MLG129
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 of Anesthesia MLG143
Malignant Hyperthermia Susceptibility MLG086
Malignant Hyperthermia Susceptibility 1 MLG132
Malignant Hyperthermia Susceptibility 5 MLG131
Malignant Iris Melanoma MLG070
Malignant Leptomeningeal Tumor MLG071
Malignant Leydig Cell Tumor MLG072
Malignant Melanoma, Somatic MLG108
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 Ovary MLG128
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
Malouf Syndrome MLF002
Mammary Paget's Disease MMM001
Mammary-Digital-Nail Syndrome MMM002
Man1b1-Cdg MN1002
Mandibular Cancer MND001
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome MND021
Mandibuloacral Dysplasia MND007
Mandibuloacral Dysplasia with Type B Lipodystrophy MND002
Mandibulofacial Dysostosis with Alopecia MND025
Mandibulofacial Dysostosis, Guion-Almeida Type MND020
Manitoba Oculotrichoanal Syndrome MNT006
Mannose-Binding Lectin Protein Deficiency MNN041
Mannosidosis MNN018
Mannosidosis, Alpha-, Types I and Ii MNN025
Mannosidosis, Beta MNN044
Mansonelliasis MNS001
Mantle Cell Lymphoma MNT001
Maoa-Related Behavior Disorders MRL005
Map2k1-Related Cardiofaciocutaneous Syndrome MP2001
Map2k1-Related Noonan Syndrome MP2002
Map2k2-Related Cardiofaciocutaneous Syndrome MP2003
Map3k1-Related 46,xy Dsd and 46,xy Cgd MP3001
Maple Syrup Urine Disease, Mild Variant MPL011
Maple Syrup Urine Disease, Type Ii MPL012
Mapt-Related Disorders MPT001
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
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
Mastl-Related Thrombocytopenia 2 MST015
Mastoiditis MST019
Maternal 14q32.2 Hypermethylation Syndrome MTR056
Maternal 14q32.2 Microdeletion Syndrome MTR055
Maternal Uniparental Disomy of Chromosome 1 MTR051
Maternal Uniparental Disomy of Chromosome 16 MTR067
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 6 MTR071
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 Ix MTR072
Maturity-Onset Diabetes of the Young, Type Vii MTR070
Maturity-Onset Diabetes of the Young, Type Viii MTR073
Max-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome MXR002
Max-Related Susceptibility to Pheochromocytoma MXR001
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-Hegglin Anomaly MYH001
May-Thurner Syndrome MYT019
Mayer-Rokitansky-Kuster-Hauser Syndrome MYR002
Mazabraud Syndrome MZB001
Mbd5 Haploinsufficiency MBD001
Mc1r-Related Cutaneous Malignant Melanoma MC1001
Mcardle Disease MCR264
Mccc1-Related 3-Methylcrotonyl-Coa Carboxylase Deficiency MCC007
Mccc2-Related 3-Methylcrotonyl-Coa Carboxylase Deficiency MCC008
Mccune-Albright Syndrome, Somatic, Mosaic MCC010
Mcee-Related Methylmalonic Acidemia MCR097
Mckusick-Kaufman Syndrome MCK005
Mcleod Syndrome with or Without Chronic Granulomatous Disease MCL055
Mct8-Specific Thyroid Hormone Cell-Membrane Transporter Deficiency MCT002
Meacham Syndrome MCH011
Measles MSL001
Mechanical Ectropion MCH001
Mechanical Strabismus MCH006
Meckel Syndrome 1 MCK022
Meckel Syndrome 10 MCK023
Meckel Syndrome 11 MCK027
Meckel Syndrome 12 MCK026
Meckel Syndrome 13 MCK028
Meckel Syndrome 2 MCK025
Meckel Syndrome 3 MCK024
Meckel Syndrome 4 MCK017
Meckel Syndrome 5 MCK019
Meckel Syndrome 6 MCK016
Meckel Syndrome 7 MCK015
Meckel Syndrome 8 MCK018
Meckel Syndrome 9 MCK021
Meckel's Diverticulum MCK002
Meconium Aspiration Syndrome MCN007
Meconium Ileus MCN017
Mecp2-Related Angelman-Like Syndrome MCP021
Mecp2-Related Disorders MCP017
Mecp2-Related Severe Neonatal Encephalopathy MCP022
Med12-Related Disorders MD1001
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
Mednik Syndrome MDN005
Medullary Cystic Kidney Disease 1 MDL008
Medullary Cystic Kidney Disease 2 MDL021
Medullary Sponge Kidney MDL009
Medullary Thyroid Carcinoma, Familial MDL022
Medulloblastoma MDL005
Medulloblastoma, Ptch2-Related MDL025
Medulloblastoma, Sufu-Related MDL011
Medulloepithelioma MDL002
Medullomyoblastoma MDL003
Meesmann Corneal Dystrophy MSM001
Meester-Loeys Syndrome MST021
Mef2a-Related Coronary Artery Disease Susceptibility MF2001
Megacolon MGC001
Megaesophagus MGS001
Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) MGK005
Megakaryocytic Leukemia MGK001
Megalencephalic Leukoencephalopathy with Subcortical Cysts MGL002
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, Somatic MGL023
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 MGL030
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2 MGL028
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3 MGL029
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome, Somatic MGL024
Megaloblastic Anemia MGL001
Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency MGL012
Megaloblastic Anemia-1, Finnish Type MGL016
Megalocornea MGL003
Megalocornea 1, X-Linked MGL026
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
Meige Syndrome MGS004
Melancholia MLN003
Melanoacanthoma MLN005
Melanocytic Nevus Syndrome, Congenital, Somatic MLN054
Melanoma MLN008
Melanoma and Neural System Tumor Syndrome MLN012
Melanoma Metastasis MLN013
Melanoma of Soft Tissue MLN064
Melanoma-Associated Retinopathy MLN046
Melanoma, Cutaneous Malignant 10 MLN055
Melanoma, Cutaneous Malignant 8 MLN043
Melanoma, Cutaneous Malignant, 2 MLN032
Melanoma, Cutaneous Malignant, 3 MLN050
Melanoma, Cutaneous Malignant, 5 MLN052
Melanoma, Cutaneous Malignant, 6 MLN051
Melanoma, Cutaneous Malignant, 9 MLN049
Melanoma, Uveal 1 MLN039
Melanoma, Uveal 2 MLN041
Melanomatosis MLN002
Melanotic Medulloblastoma MLN004
Melanotic Neurilemmoma MLN009
Melanotic Neuroectodermal Tumor MLN001
Melas, Mt-Nd1-Related MLS003
Melas, Mt-Nd5-Related MLS004
Melas, Mt-Nd6-Related MLS005
Melas, Mt-Tf-Related MLS006
Melas, Mt-Th-Related MLS012
Melas, Mt-Tk-Related MLS007
Melas, Mt-Tl1-Related MLS008
Melas, Mt-Tq-Related MLS009
Melas, Mt-Ts1-Related MLS010
Meleda Disease MLD003
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
Mend Syndrome MND023
Meniere's Disease MNR002
Meningeal Melanocytoma MNN001
Meningeal Melanoma MNN010
Meningeal Melanomatosis MNN008
Meninges Hemangiopericytoma MNN006
Meninges Sarcoma MNN011
Meningioma, Familial MNN043
Meningioma, Familial Susceptibility MNN045
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
Mental Depression MNT002
Mental Retardation 105 MNT293
Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects MNT266
Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia MNT046
Mental Retardation Epilepsy MNT014
Mental Retardation with Language Impairment and Autistic Features MNT069
Mental Retardation with Language Impairment and with or Without Autistic Features MNT237
Mental Retardation-Hypotonic Facies Syndrome, X-Linked MNT061
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 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 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 6 MNT144
Mental Retardation, Autosomal Dominant 7 MNT185
Mental Retardation, Autosomal Dominant 8 MNT168
Mental Retardation, Autosomal Dominant, 27 MNT209
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 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 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, 37 MNT169
Mental Retardation, Autosomal Recessive, 52 MNT276
Mental Retardation, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity MNT038
Mental Retardation, Fra12a Type MNT107
Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations MNT053
Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis MNT112
Mental Retardation, X-Linked 1/78 MNT292
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 106 MNT294
Mental Retardation, X-Linked 12/35 MNT249
Mental Retardation, X-Linked 23 MNT204
Mental Retardation, X-Linked 29 and Others MNT189
Mental Retardation, X-Linked 3 MNT149
Mental Retardation, X-Linked 30/47 MNT203
Mental Retardation, X-Linked 42 MNT205
Mental Retardation, X-Linked 49/15 MNT288
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 9/44 MNT291
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 Syndromic 5 MNT230
Mental Retardation, X-Linked Syndromic, Christianson Type MNT121
Mental Retardation, X-Linked Syndromic, Lubs Type MNT208
Mental Retardation, X-Linked Syndromic, Nascimento-Type MNT231
Mental Retardation, X-Linked Syndromic, Raymond Type MNT232
Mental Retardation, X-Linked Syndromic, Turner Type MNT139
Mental Retardation, X-Linked, Fraxe Type MNT068
Mental Retardation, X-Linked, Snyder-Robinson Type MNT054
Mental Retardation, X-Linked, Syndromic 11, Shashi Type MNT297
Mental Retardation, X-Linked, Syndromic 13 MNT135
Mental Retardation, X-Linked, Syndromic 15 MNT109
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, Borck Type MNT268
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, Martin-Probst Type MNT146
Mental Retardation, X-Linked, Syndromic, Wilson-Turner Type MNT260
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 Growth Hormone Deficiency MNT059
Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency MNT119
Mental Retardation, X-Linked, with Short Stature, Small Testes, Muscle Wasting, and Tremor MNT060
Mental Retsrdation, X-Linked Syndromic, Female Restricted MNT261
Mephenytoin Poor Metabolizer MPH001
Mercaptolactate-Cysteine Disulfiduria MRC009
Mercury Poisoning MRC003
Merkel Cell Carcinoma MRK001
Merrf/melas Overlap Syndrome MRR006
Mertk-Related Retinitis Pigmentosa MRT008
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, Somatic MST016
Mesp2-Related Spondylocostal Dysostosis, Autosomal Recessive MSP002
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 Sap-B Deficiency MTC067
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, Murk Jansen Type MTP026
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
Metatropic Dysplasia MTT002
Metatypical Basal Cell Carcinoma MTT001
Methanol Poisoning MTH047
Methemoglobinemia MTH007
Methemoglobinemia, Beta-Globin Type MTH064
Methemoglobinemia, Type I MTH037
Methemoglobinemia, Type Iv MTH036
Methionine Adenosyltransferase Deficiency MTH011
Methotrexate Toxicity or Dose Selection MTH061
Methylmalonate Semialdehyde Dehydrogenase Deficiency MTH013
Methylmalonic Acidemia MTH008
Methylmalonic Acidemia Due to Transcobalamin Receptor Defect MTH069
Methylmalonic Acidemia with Homocystinuria MTH021
Methylmalonic Acidemia with Homocystinuria Type Cbld MTH066
Methylmalonic Acidemia with Homocystinuria Type Cblj MTH067
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, Mut(0) Type MTH039
Methylmalonic Aciduria, Transient, Due to Transcobalamin Receptor Defect MTH068
Methylmalonic Aciduria, Vitamin B12-Responsive MTH033
Methylmalonic Aciduria, Vitamin B12-Responsive, Due to Defect in Synthesis of Adenosylcobalamin, Cblb Complementation Type MTH034
Methylmalonyl-Coa Epimerase Deficiency MTH040
Methylmalonyl-Coenzyme a Mutase Deficiency MTH025
Mevalonic Aciduria MVL001
Mfap5-Related Thoracic Aortic Aneurysms and Aortic Dissections MFP001
Mhc Class Ii Deficiency MHC001
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 2, Primary, Autosomal Recessive, with or Without Cortical Malformations MCR222
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 Polymicrogyria MCR275
Microcephaly-Capillary Malformation Syndrome MCR183
Microcephaly-Complex Motor and Sensory Axonal Neuropathy Syndrome MCR298
Microcephaly-Micromelia Syndrome MCR326
Microcephaly-Polymicrogyria-Corpus Callosum Agenesis Syndrome MCR285
Microcephaly, Amish Type MCR257
Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis MCR315
Microcephaly, Cortical Malformations, and Mental Retardation MCR098
Microcephaly, Epilepsy, and Diabetes Syndrome MCR209
Microcephaly, Postnatal Progressive, with Seizures and Brain Atrophy MCR123
Microcephaly, Progressive, Seizures, and Cerebral and Cerebellar Atrophy MCR226
Microcephaly, Seizures, and Developmental Delay MCR064
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 Seizures MCR325
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 Coloboma 3 MCR136
Microphthalmia with Coloboma 5 MCR127
Microphthalmia with Coloboma 6, Digenic MCR110
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 Coloboma 10 MCR271
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 1, Susceptibility MCR276
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
Microvillus Inclusion Disease MCR094
Mid-Dermal Elastolysis MDD015
Middle Cerebral Artery Infarction MDD003
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 3 MGR022
Migraine with or Without Aura 5 MGR024
Migraine with or Without Aura 6 MGR033
Migraine with or Without Aura, Susceptibility 13 MGR034
Migraine Without Aura 4 MGR023
Migraine, Familial Hemiplegic, 1 MGR032
Migraine, Familial Hemiplegic, 2 MGR030
Migraine, Familial Hemiplegic, 3 MGR031
Migraine, with or Without Aura 13 MGR019
Mikulicz Disease MKL001
Mild Canavan Disease MLD009
Mild Hemophilia a MLD013
Mild Hemophilia B MLD014
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 Syndrome MLL012
Miller-Dieker Lissencephaly Syndrome MLL018
Mineral Metabolism Disease MNR003
Minicore Myopathy with External Ophthalmoplegia MNC011
Minimal Pigment Oculocutaneous Albinism Type 1 MNM005
Mir184 MR1001
Mirage Syndrome MRG013
Mirror Movements 1 and/or Agenesis of the Corpus Callosum MRR014
Mirror Movements 2 MRR010
Mirror Movements 3 MRR012
Mismatch Repair Cancer Syndrome MSM014
Mitchell-Riley Syndrome MTC096
Mite Infestation MTN002
Mitf-Related Susceptibility to Cutaneous Malignant Melanoma MTF002
Mitochondrial Cardiomyopathy MTC028
Mitochondrial Complex Deficiency, Nuclear Type 4 MTC092
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
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 5 MTC099
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, Nuclear Type 1 MTC029
Mitochondrial Complex V Deficiency, Nuclear Type 2 MTC068
Mitochondrial Complex V Deficiency MTC021
Mitochondrial Complex V Deficiency, Mitochondrial 1 MTC080
Mitochondrial Complex V Deficiency, Mitochondrial 2 MTC082
Mitochondrial Disorders MTC069
Mitochondrial Dna Depletion Syndrome 1 MTC061
Mitochondrial Dna Depletion Syndrome 11 MTC078
Mitochondrial Dna Depletion Syndrome 12a Ad MTC127
Mitochondrial Dna Depletion Syndrome 12b Ar MTC128
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, Encephalomyopathic Form MTC033
Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form MTC034
Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form MTC093
Mitochondrial Dna Depletion Syndrome, Mgme1-Related MTC130
Mitochondrial Dna Depletion Syndrome, Mngie Form MTC084
Mitochondrial Dna Depletion Syndrome, Myopathic Form MTC035
Mitochondrial Dna-Associated Leigh Syndrome and Narp MTC015
Mitochondrial Encephalomyopathy MTC004
Mitochondrial Infantile Bilateral Striatal Necrosis MTC081
Mitochondrial Membrane Protein-Associated Neurodegeneration MTC036
Mitochondrial Metabolism Disease MTC005
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 Recessive Ataxia Syndrome MTC057
Mitochondrial Respiratory Chain Complex Ii Deficiency, Sdha-Related MTC042
Mitochondrial Respiratory Chain Complex Ii Deficiency, Sdhaf1-Related MTC041
Mitochondrial Respiratory Chain Complex Ii Deficiency, Sdhd-Related MTC117
Mitochondrial Respiratory Chain Complex Iii Deficiency, Bcs1l-Related MTC044
Mitochondrial Respiratory Chain Complex Iii Deficiency, Cyc1-Related MTC120
Mitochondrial Respiratory Chain Complex Iii Deficiency, Lyrm7-Related MTC121
Mitochondrial Respiratory Chain Complex Iii Deficiency, Ttc19-Related MTC045
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcc2-Related MTC122
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcc3-Related MTC123
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcrb-Related MTC046
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcrq Related MTC047
Mitochondrial Respiratory Chain Complex Iii Deficiency, Uqcrq2 Related MTC110
Mitochondrial Respiratory Chain Complex Iii, Cytochrome B Subunit MTC048
Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency MTC108
Mitral Atresia MTR027
Mitral Valve Disease MTR012
Mitral Valve Insufficiency MTR002
Mitral Valve Prolapse 2 MTR077
Mitral Valve Prolapse, Myxomatous 1 MTR040
Mitral Valve Prolapse, Myxomatous 3 MTR042
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 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
Mkks-Related Bardet-Biedl Syndrome MKK001
Mks1-Related Bardet-Biedl Syndrome MKS001
Mks1-Related Meckel Syndrome MKS002
Mlc1-Related Megalencephalic Leukoencephalopathy with Subcortical Cysts MLC001
Mlh1-Related Lynch Syndrome MLH002
Mlh1-Related Muir-Torre Syndrome MLH003
Mlh1-Related Turcot Syndrome MLH004
Mlh3-Related Lynch Syndrome MLH005
Mmaa-Related Methylmalonic Acidemia MMR001
Mmab-Related Methylmalonic Acidemia MMB004
Mmadhc-Related Methylmalonic Acidemia MMD001
Mmp21-Related Visceral Heterotaxy MMP003
Mn1 MN1001
Moderate and Severe Traumatic Brain Injury MDR006
Moderately Severe Hemophilia a MDR007
Moderately Severe Hemophilia B MDR008
Mody, Type I MDY005
Mody, Type Ii MDY003
Mody, Type Iii MDY004
Mody, Type Iv MDY006
Moebius Syndrome MBS002
Mohr Syndrome MHR002
Mohr-Tranebjaerg Syndrome MHR001
Molluscum Contagiosum MLL001
Molybdenum Cofactor Deficiency MLY001
Molybdenum Cofactor Deficiency a MLY006
Molybdenum Cofactor Deficiency B MLY005
Molybdenum Cofactor Deficiency C MLY007
Mondini Dysplasia MND005
Mongolian Spot MNG001
Monilethrix MNL001
Monkeypox MNK002
Monocarboxylate Transporter 1 Deficiency MNC019
Monoclonal Gammopathy of Uncertain Significance MNC006
Monoclonal Paraproteinemia MNC004
Monocular Esotropia MNC001
Monocytic Leukemia MNC007
Monofixation Syndrome MNF001
Monogenic Diabetes MNG006
Monogenic Non-Syndromic Obesity, Autosomal Recessive MNG004
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 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
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 6 with Achalasia MYM008
Moyamoya Disease MYM002
Moyamoya Disease 2 MYM004
Moyamoya Disease 3 MYM005
Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism MYM012
Moyamoya Disease 5 MYM003
Mpph Syndrome MPP001
Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome MPV001
Mrpl40-Related Disorder MRP004
Ms4a1-Related Common Variable Immune Deficiency MS4001
Msh2-Related Lynch Syndrome MSH002
Msh2-Related Muir-Torre Syndrome MSH003
Msh2-Related Turcot Syndrome MSH004
Msh6-Related Lynch Syndrome MSH005
Msh6-Related Turcot Syndrome MSH006
Msx2-Related Craniosynostosis MSX001
Mt-Co1-Related Hearing Loss and Deafness MTC052
Mt-Cyb-Related Recurrent Myoglobinuria MTC053
Mt-Rnr1-Related Hearing Loss and Deafness MTR037
Mt-Ts1-Related Hearing Loss and Deafness MTT003
Mt-Tt Related Parkinson Disease Susceptibility MTT006
Mthfr Gene Mutation MTH044
Mthfr Thermolabile Variant MTH028
Mthfr-Related Altered Drug Metabolism MTH063
Mu Chain Disease MCH003
Mucinoses MCN011
Mucinous Adenocarcinoma MCN001
Mucinous Adenocarcinoma of the Appendix MCN018
Mucinous Adenofibroma MCN006
Mucinous Bronchioloalveolar Adenocarcinoma MCN021
Mucinous Cystadenocarcinoma MCN008
Mucinous Cystadenofibroma MCN010
Mucinous Intrahepatic Cholangiocarcinoma MCN005
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
Mucociliary Clearance Disorder MCC011
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 Ih MCP012
Mucopolysaccharidosis Ih/s MCP036
Mucopolysaccharidosis Ii MCP009
Mucopolysaccharidosis Iii MCP001
Mucopolysaccharidosis is MCP037
Mucopolysaccharidosis Iv MCP004
Mucopolysaccharidosis Iva MCP038
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 Iiia MCP041
Mucopolysaccharidosis Type Iiib MCP026
Mucopolysaccharidosis Type Iiic MCP020
Mucopolysaccharidosis Type Iiid MCP014
Mucopolysaccharidosis Type Ivb MCP023
Mucopolysaccharidosis Type Ix MCP015
Mucopolysaccharidosis Type Vi MCP024
Mucopolysaccharidosis Vii MCP003
Mucopolysaccharidosis-Plus Syndrome MCP040
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 of Torg MLT064
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
Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type MLT154
Multiple Acyl-Coa Dehydrogenase Deficiency, Severe Neonatal Type MLT155
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 Cutaneous and Uterine Leiomyomas MLT066
Multiple Enchondromatosis, Maffucci Type MLT145
Multiple Endocrine Neoplasia MLT074
Multiple Endocrine Neoplasia 1 MLT136
Multiple Endocrine Neoplasia Iia MLT024
Multiple Endocrine Neoplasia Iib MLT025
Multiple Endocrine Neoplasia, Type Iv MLT086
Multiple Epiphyseal Dysplasia MLT007
Multiple Epiphyseal Dysplasia Due to Collagen 9 Anomaly MLT141
Multiple Epiphyseal Dysplasia, Dominant MLT030
Multiple Epiphyseal Dysplasia, Recessive MLT031
Multiple Familial Trichoepithelioma MLT048
Multiple Fibroadenomas of the Breast MLT120
Multiple Joint Dislocations, Short Stature, Craniofacial Dysmorphism, and Congenital Heart Defects MLT123
Multiple Joint Dislocations, Short Stature, Craniofacial Dysmorphism, with or Without Congenital Heart Defects MLT153
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 Mucosal Neuroma MLT011
Multiple Myeloma MLT019
Multiple Paragangliomas Associated with Polycythemia MLT106
Multiple Personality Disorder MLT010
Multiple Pterygium Syndrome, Lethal Type MLT134
Multiple Sclerosis 2 MLT093
Multiple Sclerosis 3 MLT094
Multiple Sclerosis 4 MLT095
Multiple Sclerosis 5 MLT124
Multiple Sclerosis, Disease Progression, Modifier of MLT077
Multiple Self-Healing Squamous Epithelioma MLT152
Multiple Sulfatase Deficiency MLT135
Multiple Symmetrical Lipomatosis MLT002
Multiple Synostoses Syndrome MLT072
Multiple Synostoses Syndrome 1 MLT059
Multiple Synostoses Syndrome 2 MLT060
Multiple Synostoses Syndrome 3 MLT078
Multiple System Atrophy MLT021
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 Glycogenosis MSC006
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, 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, 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-Dystroglycanopathy (congenital with Brain and Eye Anomalies, Type a, 11 MSC094
Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies, Type a, 8 MSC096
Muscular Dystrophy, Congenital MSC124
Muscular Dystrophy, Congenital Merosin-Deficient MSC039
Muscular Dystrophy, Congenital, 1b MSC050
Muscular Dystrophy, Congenital, Davignon-Chauveau Type MSC141
Muscular Dystrophy, Congenital, Due to Itga7 Deficiency MSC052
Muscular Dystrophy, Congenital, Megaconial Type MSC028
Muscular Dystrophy, Congenital, Merosin-Positive MSC029
Muscular Dystrophy, Congenital, with Cataracts and Intellectual Disability MSC142
Muscular Dystrophy, Limb-Girdle, Type 1a MSC115
Muscular Dystrophy, Limb-Girdle, Type 1b MSC112
Muscular Dystrophy, Limb-Girdle, Type 1e MSC117
Muscular Dystrophy, Limb-Girdle, Type 1f MSC057
Muscular Dystrophy, Limb-Girdle, Type 1g MSC138
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 2y MSC135
Muscular Dystrophy, Limb-Girdle, Type 2z MSC137
Muscular Dystrophy, Limb-Girdle, Type Ic MSC049
Muscular Dystrophy, Rigid Spine, 1 MSC051
Muscular Phosphorylase Kinase Deficiency MSC031
Musculocontractural Ehlers-Danlos Syndrome MSC134
Musk-Related Congenital Myasthenic Syndrome MSK001
Mut-Related Methylmalonic Acidemia MTR038
Mutagen Sensitivity MTG002
Mutism MTS001
Mutyh-Associated Polyposis MTY001
Myasthenia Gravis MYS003
Myasthenia Gravis Congenital MYS011
Myasthenia Gravis with Thymus Hyperplasia MYS007
Myasthenia, Congenital, 12, with Tubular Aggregates MYS045
Myasthenia, Limb-Girdle, with Tubular Aggregates MYS015
Myasthenic Syndrome, Congenital, 10 MYS052
Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency MYS057
Myasthenic Syndrome, Congenital, 13, with Tubular Aggregates MYS058
Myasthenic Syndrome, Congenital, 14, with Tubular Aggregates MYS053
Myasthenic Syndrome, Congenital, 15, Without Tubular Aggregates MYS043
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, with Pre- and Postsynaptic Defects MYS042
Myasthenic Syndrome, Congenital, 9, Associated with Acetylcholine Receptor Deficiency MYS054
Mybpc3-Related Dilated Cardiomyopathy MYB002
Mybpc3-Related Familial Hypertrophic Cardiomyopathy MYB003
Mycetoma MYC012
Mycobacterium Abscessus MYC013
Mycobacterium Avium Complex Disease MYC002
Mycobacterium Chelonae MYC014
Mycobacterium Fortuitum MYC015
Mycobacterium Gordonae MYC016
Mycobacterium Kansasii MYC017
Mycobacterium Malmoense MYC018
Mycobacterium Marinum MYC019
Mycobacterium Tuberculosis 2 MYC054
Mycobacterium Tuberculosis 3 MYC055
Mycobacterium Tuberculosis, Susceptibility to Infection by MYC020
Mycoplasmal Pneumonia MYC022
Mycosis Fungoides MYC006
Myd88 Deficiency MYD002
Myelitis MYL001
Myelocystocele MYL044
Myelodysplasia and Leukemia Syndrome with Monosomy 7 MYL048
Myelodysplastic Myeloproliferative Cancer MYL004
Myelodysplastic Syndrome MYL009
Myelodysplastic Syndrome, Susceptibility, Gata2-Related MYL039
Myelofibrosis with Myeloid Metaplasia, Somatic MYL045
Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities MYL054
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
Myeloid/lymphoid or Mixed Lineage Leukemia MYL055
Myelomeningocele MYL020
Myelopathy, Htlv-1-Associated MYL057
Myeloperoxidase Deficiency MYL013
Myelophthisic Anemia MYL002
Myeloproliferative Disorder with Eosinophilia MYL015
Myeloproliferative Neoplasm MYL031
Myeloproliferative Neoplasms, Familial MYL052
Myeloproliferative Syndrome, Transient MYL058
Myeloproliferative/lymphoproliferative Neoplasms, Familial MYL064
Myh-9 Related Disease MYH015
Myh11-Related Thoracic Aortic Aneurysms and Aortic Dissections MYH005
Myh3-Related Arthrogryposis Multiplex Congenita, Distal, Type 2b MYH006
Myh6-Related Dilated Cardiomyopathy MYH007
Myh6-Related Familial Hypertrophic Cardiomyopathy MYH008
Myh7-Related Congenital Fiber-Type Disproportion MYH013
Myh7-Related Dilated Cardiomyopathy MYH009
Myh7-Related Familial Hypertrophic Cardiomyopathy MYH010
Myh7-Related Myosin Storage Myopathy MYH011
Myh9 Related Thrombocytopenia MYH004
Myhre Syndrome MYH012
Myiasis MYS004
Myl2-Related Familial Hypertrophic Cardiomyopathy MYL021
Myl3-Related Familial Hypertrophic Cardiomyopathy MYL022
Myl4-Related Familial Atrial Fibrillation MYL063
Mylk-Related Thoracic Aortic Aneurysms and Aortic Dissections MYL023
Myoblastoma MYB001
Myocardial Infarction MYC007
Myocardial Infarction 2 MYC058
Myocardial Infarction, Susceptibility to, 1 MYC029
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, Infantile, Familial MYC048
Myoclonic Epilepsy, Juvenile 1 MYC070
Myoclonic-Astastic Epilepsy MYC069
Myoclonic-Atonic Epilepsy MYC071
Myoclonus MYC033
Myoclonus Epilepsy MYC026
Myoclonus, Familial Cortical MYC066
Myoclonus, Intractable, Neonatal MYC075
Myoepithelial Carcinoma MYP002
Myofascial Pain Syndrome MYF002
Myofibrillar Myopathy MYF003
Myofibroma MYF001
Myofibromatosis, Infantile 2 MYF008
Myofibromatosis, Infantile, 1 MYF007
Myoglobinuria MYG005
Myoglobinuria Recurrent MYG003
Myoglobinuria, Acute Recurrent, Autosomal Recessive MYG004
Myokymia 1 with or Without Hypomagnesemia MYK003
Myoma MYM001
Myopathic Intestinal Pseudoobstruction MYP066
Myopathy MYP004
Myopathy Due to Myoadenylate Deaminase Deficiency MYP071
Myopathy of Extraocular Muscle MYP005
Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme MYP025
Myopathy with Deficiency of Iscu MYP009
Myopathy with Extrapyramidal Signs MYP086
Myopathy with Lactic Acidosis, Hereditary MYP097
Myopathy, Areflexia, Respiratory Distress, and Dysphagia, Early-Onset MYP093
Myopathy, Centronuclear, 3 MYP096
Myopathy, Centronuclear, 4 MYP098
Myopathy, Centronuclear, Autosomal Recessive MYP102
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, 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, 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, Myofibrillar, Fatal Infantile Hypertrophy, Alpha-B Crystallin-Related MYP083
Myopathy, Myosin Storage, Autosomal Dominant MYP105
Myopathy, Myosin Storage, Autosomal Recessive MYP106
Myopathy, Proximal, with Early Respiratory Muscle Involvement MYP103
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 10 MYP044
Myopia 14 MYP069
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 6 MYP018
Myopia 7 MYP040
Myopia 8 MYP041
Myopia 9 MYP048
Myopia, High, with Cataract and Vitreoretinal Degeneration MYP073
Myopia, X-Linked MYP024
Myosclerosis, Congenital MYS021
Myosin Storage Myopathy MYS032
Myositis MYS005
Myositis Fibrosa MYS002
Myositis Ossificans MYS001
Myostatin-Related Muscle Hypertrophy MYS010
Myotonia MYT011
Myotonia Congenita MYT023
Myotonia Congenita, Atypical, Acetazolamide-Responsive MYT015
Myotonia Congenita, Dominant MYT013
Myotonia Congenita, Recessive MYT012
Myotonic Disease MYT003
Myotonic Dystrophy MYT002
Myotonic Dystrophy 1 MYT021
Myotonic Dystrophy 2 MYT020
Myotubular Myopathy with Abnormal Genital Development MYT025
Myotubular Myopathy, X-Linked MYT022
Myoz2-Related Familial Hypertrophic Cardiomyopathy MYZ001
Mypn-Related Cardiomyopathy MYP109
Mypn-Related Familial Restrictive Cardiomyopathy MYP115
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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