| Disease Name |
Symbol |
Acronym |
| Machado-joseph Disease |
MCH002 |
|
| Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies |
MCR021 |
|
| Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis |
MCR095 |
MAC |
| Macrocephaly/autism Syndrome |
MCR096 |
|
| Macrocytic Anemia |
MCR017 |
|
| Macroglobulinemia |
MCR004 |
|
| Macroglossia |
MCR037 |
|
| Macrostomia |
MCR105 |
|
| Macrothrombocytopenia |
MCR022 |
|
| Macrothrombocytopenia and Progressive Sensorineural Deafness |
MCR139 |
|
| Macrothrombocytopenia Progressive Deafness |
MCR041 |
|
| Macular Corneal Dystrophy |
MCL002 |
|
| Macular Degeneration |
MCL005 |
|
| Macular Degeneration, Age-related, 10 |
MCL030 |
|
| Macular Degeneration, Age-related, 11 |
MCL032 |
|
| Macular Degeneration, Age-related, Reduced Risk of |
MCL033 |
|
| Macular Degeneration, X-linked Atrophic |
MCL029 |
|
| Macular Dystrophy |
MCL007 |
|
| Macular Dystrophy, Atypical Vitelliform |
MCL017 |
VMD1 |
| Macular Dystrophy, Autosomal Dominant, Chromosome 6-linked |
MCL025 |
|
| Macular Dystrophy, Dominant Cystoid |
MCL027 |
|
| Macular Dystrophy, Patterned |
MCL034 |
|
| Macular Dystrophy, Retinal, 2 |
MCL035 |
|
| Macular Dystrophy, Retinal, 3 |
MCL026 |
|
| Macular Holes |
MCL003 |
|
| Macular Retinal Edema |
MCL006 |
|
| Maculopathy |
MCL008 |
|
| Majeed Syndrome |
MJD001 |
|
| Major Affective Disorder |
MJR002 |
|
| Major Affective Disorder 1 |
MJR007 |
|
| Major Affective Disorder 2 |
MJR008 |
|
| Major Affective Disorder 3, Early Onset |
MJR009 |
|
| Major Affective Disorder 4 |
MJR004 |
|
| Major Affective Disorder 5 |
MJR006 |
|
| Major Affective Disorder 6 |
MJR003 |
|
| Major Affective Disorder-7 |
MJR018 |
|
| Major Affective Disorder-8 |
MJR020 |
|
| Major Affective Disorder-9 |
MJR019 |
|
| Major Depressive Disorder |
MJR001 |
|
| Major Depressive Disorder 1 |
MJR013 |
|
| Major Depressive Disorder 2 |
MJR014 |
|
| Major Depressive Disorder, Response to Citalopram Therapy in |
MJR012 |
|
| Malaria |
MLR004 |
|
| Malaria, Cerebral, Reduced Risk of |
MLR013 |
|
| Malaria, Intensity of Infection |
MLR014 |
|
| Malaria, Mild |
MLR020 |
|
| Malaria, Protection Against |
MLR018 |
|
| Malaria, Resistance to |
MLR012 |
|
| Malaria, Severe, Resistance to |
MLR016 |
|
| Malaria, Vivax, Protection Against |
MLR015 |
|
| Male Breast Cancer |
MLB002 |
|
| Male Germ Cell Tumor |
MLG083 |
|
| Male Infertility |
MLN007 |
|
| Male Infertility Due to Acrosin Deficiency |
MLN010 |
|
| Male Pseudohermaphroditism Due to Defective Lh |
MLP001 |
|
| Malignant Biphasic Mesothelioma |
MLG011 |
|
| Malignant Conjunctiva Melanoma |
MLG016 |
|
| Malignant Cylindroma |
MLG087 |
|
| Malignant Ependymoma |
MLG064 |
|
| Malignant Epithelial Mesothelioma |
MLG012 |
|
| Malignant Essential Hypertension |
MLG039 |
|
| Malignant Fibrous Histiocytoma |
MLG084 |
|
| Malignant Fibrous Histiocytoma of Bone |
MLG014 |
|
| Malignant Fibroxanthoma |
MLG065 |
MFH |
| Malignant Germ Cell Tumor |
MLG088 |
|
| Malignant Giant Cell Tumor |
MLG067 |
|
| Malignant Giant Cell Tumor of Soft Parts |
MLG018 |
|
| Malignant Glioma |
MLG068 |
|
| Malignant Granular Cell Myoblastoma |
MLG032 |
|
| Malignant Histiocytosis |
MLG054 |
|
| Malignant Hypertension |
MLG069 |
|
| Malignant Hyperthermia |
MLG056 |
MH |
| Malignant Hyperthermia Susceptibility |
MLG086 |
|
| Malignant Hyperthermia Susceptibility Type 1 |
MLG090 |
MHS |
| Malignant Hyperthermia Susceptibility Type 5 |
MLG094 |
MHS5 |
| Malignant Mesenchymal Tumor |
MLG097 |
|
| Malignant Mesothelioma |
MLG075 |
|
| Malignant Mixed Mullerian Tumor |
MLG098 |
|
| Malignant Neoplasm of Cerebellum |
MLG102 |
|
| Malignant Ovarian Brenner Tumor |
MLG053 |
|
| Malignant Ovarian Cyst |
MLG033 |
|
| Malignant Peripheral Nerve Sheath Tumor |
MLG077 |
MPNST |
| Malignant Peritoneal Mesothelioma |
MLG002 |
|
| Malignant Pleural Mesothelioma |
MLG079 |
|
| Malignant Sertoli Cell Tumor |
MLG022 |
|
| Malignant Skin Fibrous Histiocytoma |
MLG007 |
|
| Malignant Spindle Cell Melanoma |
MLG005 |
|
| Malignant Struma Ovarii |
MLG059 |
|
| Malignant Syringoma |
MLG049 |
|
| Malignant Teratoma |
MLG081 |
|
| Malignant Triton Tumor |
MLG041 |
|
| Malonyl-coa Decarboxylase Deficiency |
MLN011 |
|
| Malt Lymphoma |
MLT022 |
|
| Mammary Duct Ectasia |
MMM003 |
|
| Mammary Paget's Disease |
MMM001 |
|
| Mammary-digital-nail Syndrome |
MMM002 |
|
| Mandibuloacral Dysplasia |
MND007 |
|
| Mandibuloacral Dysplasia with Type a Lipodystrophy |
MND003 |
MADA |
| Mandibuloacral Dysplasia with Type B Lipodystrophy |
MND002 |
MADB |
| Manic-depressive Illness |
MNC008 |
|
| Manitoba Oculotrichoanal Syndrome |
MNT006 |
MOTA |
| Mannose-binding Protein Deficiency |
MNN023 |
|
| Mannosidase Deficiency Disease |
MNN030 |
|
| Mannosidosis |
MNN018 |
|
| Mannosidosis, Alpha-, Types I and Ii |
MNN025 |
|
| Mantle Cell Lymphoma |
MNT001 |
|
| Maple Syrup Urine Disease |
MPL001 |
MSUD |
| Maple Syrup Urine Disease Type 1a |
MPL003 |
|
| Maple Syrup Urine Disease Type 2 |
MPL005 |
MSUD2 |
| Maple Syrup Urine Disease, Type Ia |
MPL008 |
|
| Maple Syrup Urine Disease, Type Ib |
MPL009 |
|
| Mapt-related Disorders |
MPT001 |
|
| Marantic Endocarditis |
MRN001 |
|
| Marasmus |
MRS001 |
|
| Marek Disease |
MRK002 |
|
| Marfan Syndrome |
MRF001 |
MFS |
| Marfan-like Connective Tissue Disorder |
MRF002 |
|
| Marginal Zone B-cell Lymphoma |
MRG003 |
|
| Marinesco-sjogren Syndrome |
MRN003 |
MSS |
| Marshall Syndrome |
MRS002 |
|
| Marshall-smith Syndrome |
MRS004 |
|
| Martin-probst Deafness-mental Retardation Syndrome |
MRT002 |
|
| Martsolf Syndrome |
MRT007 |
|
| Masa Syndrome |
MSS001 |
|
| Mass Syndrome |
MSS002 |
OCTD |
| Mast Cell Neoplasm |
MST004 |
|
| Mast Syndrome |
MST006 |
HSP21 |
| Mast-cell Leukemia |
MST002 |
|
| Mast-cell Sarcoma |
MST001 |
|
| Masters-allen Syndrome |
MST003 |
|
| Mastitis |
MST005 |
|
| Mastocytosis |
MST009 |
|
| Mastocytosis with Associated Hematologic Disorder |
MST007 |
|
| Maternal Hyperphenylalaninemia |
MTR016 |
MPKU |
| Maternal Uniparental Disomy, Chromosome 14 |
MTR034 |
|
| Maternally Inherited Leigh Syndrome |
MTR017 |
MILS |
| Mature B-cell Neoplasm |
MTR008 |
|
| Mature Cataract |
MTR001 |
TOTAL |
| Mature T-cell and Nk-cell Neoplasm |
MTR009 |
|
| Mature Teratoma |
MTR010 |
|
| Maturity-onset Diabetes of the Young |
MTR004 |
MODY |
| Maturity-onset Diabetes of the Young, Type 1 |
MTR018 |
MODY1 |
| Maturity-onset Diabetes of the Young, Type 2 |
MTR019 |
MODY2 |
| 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 3 |
MTR020 |
MODY3 |
| Maturity-onset Diabetes of the Young, Type 4 |
MTR021 |
MODY4 |
| Maturity-onset Diabetes of the Young, Type 5 |
MTR022 |
RCAD |
| Maturity-onset Diabetes of the Young, Type 6 |
MTR023 |
MODY6 |
| Maturity-onset Diabetes of the Young, Type 7 |
MTR024 |
MODY7 |
| Maturity-onset Diabetes of the Young, Type 8 |
MTR025 |
DPED |
| Maturity-onset Diabetes of the Young, Type 9 |
MTR026 |
MODY9 |
| Maxillary Sinus Adenoid Cystic Carcinoma |
MXL002 |
|
| Maxillary Sinus Cancer |
MXL008 |
|
| Maxillary Sinus Squamous Cell Carcinoma |
MXL004 |
|
| May-hegglin Anomaly |
MYH001 |
|
| Mayer-rokitansky-kuster-hauser Syndrome |
MYR002 |
CAUV |
| Mccune Albright Syndrome |
MCC001 |
MAS |
| Mckusick-kaufman Syndrome |
MCK005 |
MKS |
| Mcleod Neuroacanthocytosis Syndrome |
MCL014 |
|
| Mcleod Syndrome |
MCL009 |
|
| Mcleod Syndrome with Neuroacanthosis |
MCL010 |
|
| Meacham Syndrome |
MCH011 |
|
| Mean Platelet Volume Qtl1 |
MNP002 |
|
| Mean Platelet Volume Qtl2 |
MNP003 |
|
| Mean Platelet Volume Qtl3 |
MNP004 |
|
| Measles |
MSL001 |
|
| Meckel Syndrome |
MCK006 |
MKS |
| Meckel Syndrome 7 |
MCK015 |
|
| Meckel Syndrome Type 2 |
MCK008 |
MKS2 |
| Meckel Syndrome Type 3 |
MCK009 |
MKS3 |
| Meckel Syndrome Type 4 |
MCK011 |
|
| Meckel Syndrome, Type 1 |
MCK013 |
|
| Meckel Syndrome, Type 5 |
MCK014 |
|
| Meckel Syndrome, Type 6 |
MCK012 |
|
| Meckel's Diverticulum |
MCK002 |
|
| Meconium Aspiration Syndrome |
MCN007 |
MAS |
| Meconium Ileus in Cystic Fibrosis |
MCN015 |
|
| Median Neuropathy |
MDN002 |
|
| Median Rhomboid Glossitis |
MDN001 |
|
| Mediastinal Neoplasm |
MDS025 |
|
| Mediastinitis |
MDS022 |
|
| Medium-chain Acyl-coenzyme a Dehydrogenase Deficiency |
MDM001 |
MCADD |
| Medullary Cystic Kidney Disease 1 |
MDL008 |
MCKD1 |
| Medullary Sponge Kidney |
MDL009 |
|
| Medulloblastoma |
MDL005 |
MDB |
| Medulloepithelioma |
MDL002 |
|
| Medullomyoblastoma |
MDL003 |
|
| Meesmann Corneal Dystrophy |
MSM001 |
MECD |
| Megacolon |
MGC001 |
|
| Megacystis-microcolon-intestinal Hypoperistalsis Syndrome |
MGC002 |
MMIHS |
| Megaesophagus |
MGS001 |
|
| Megakaryoblastic Leukemia |
MGK003 |
|
| Megakaryocytic Leukemia |
MGK001 |
|
| Megakaryocytic Tumor |
MGK002 |
|
| Megalencephalic Leukoencephalopathy with Subcortical Cysts |
MGL002 |
VL |
| Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 |
MGL009 |
|
| Megalencephaly |
MGL013 |
|
| Megaloblastic Anemia |
MGL001 |
|
| Megaloblastic Anemia 1 |
MGL018 |
MGA1 |
| Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency |
MGL012 |
|
| Megaloblastic Anemia-1, Finnish Type |
MGL016 |
|
| Megaloblastic Anemia-1, Norwegian Type |
MGL014 |
|
| Megalocornea |
MGL003 |
|
| Megalocornea - Spherophakia - Secondary Glaucoma |
MGL005 |
MSPKA |
| Megalocornea, X-linked |
MGL015 |
|
| Mehmo Syndrome |
MHM001 |
|
| Meier-gorlin Syndrome |
MRG005 |
|
| Melancholia |
MLN003 |
|
| Melanoacanthoma |
MLN005 |
|
| Melanoma |
MLN008 |
|
| Melanoma and Neural System Tumor Syndrome |
MLN012 |
|
| Melanoma Astrocytoma Syndrome |
MLN016 |
|
| Melanoma Metastasis |
MLN013 |
|
| Melanoma Susceptibility 5 |
MLN021 |
|
| Melanoma, Cutaneous Malignant, 4 |
MLN023 |
|
| Melanoma, Desmoplastic Neurotrophic |
MLN025 |
|
| Melanoma, Malignant Sporadic |
MLN028 |
|
| Melanoma, Malignant, Somatic |
MLN020 |
|
| Melanomatosis |
MLN002 |
|
| Melanotic Neurilemmoma |
MLN009 |
|
| Melanotic Neuroectodermal Tumor |
MLN001 |
|
| Melas Syndrome |
MLS001 |
MELAS |
| Meleda Disease |
MLD003 |
MDM |
| Meliodosis |
MLD005 |
|
| Melioidosis |
MLD001 |
|
| Melkersson-rosenthal Syndrome |
MLK003 |
MRS |
| Melnick-needles Syndrome |
MLN014 |
MNS |
| Melorheostosis |
MLR003 |
|
| Melorheostosis with Osteopoikilosis |
MLR010 |
|
| Membranoproliferative Glomerulonephritis |
MMB001 |
|
| Membranoproliferative Glomerulonephritis with Cfh Deficiency |
MMB006 |
|
| Membranous Glomerulonephritis |
MMB002 |
MGN |
| Membranous Glomerulonephritis, Antenatal |
MMB005 |
|
| Memory Impairment |
MMR004 |
|
| Memory, Enhanced, Association with |
MMR003 |
|
| Menarche, Age at, Qtl |
MNR007 |
|
| Menarche, Age at, Qtl2 |
MNR005 |
|
| Menarche, Age at, Qtl3 |
MNR006 |
|
| Menieres Disease |
MNR008 |
|
| Meningeal Melanocytoma |
MNN001 |
|
| Meninges Hemangiopericytoma |
MNN006 |
|
| Meninges Sarcoma |
MNN011 |
|
| Meningioma |
MNN012 |
|
| Meningioma, Sis-related |
MNN026 |
|
| Meningitis |
MNN013 |
|
| Meningitis and Encephalitis |
MNN024 |
|
| Meningocele |
MNN007 |
|
| Meningococcal Infection |
MNN020 |
|
| Meningococcemia |
MNN021 |
|
| Meningoencephalitis |
MNN009 |
|
| Meningothelial Meningioma |
MNN004 |
|
| Menkes Disease |
MNK001 |
MK |
| Menopause, Natural, Age at, Qtl1 |
MNP007 |
|
| Menopause, Natural, Age at, Qtl2 |
MNP005 |
|
| Menopause, Natural, Age at, Qtl3 |
MNP006 |
|
| Menopause, Natural, Age at, Qtl4 |
MNP008 |
|
| Mental Depression |
MNT002 |
|
| Mental Disorders |
MNT062 |
|
| Mental Health Wellness-1 |
MNT102 |
|
| Mental Health Wellness-2 |
MNT103 |
|
| Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia |
MNT046 |
|
| Mental Retardation Epilepsy |
MNT014 |
|
| Mental Retardation in Cri-du-chat Syndrome |
MNT003 |
|
| Mental Retardation Progressive Spasticity |
MNT024 |
|
| Mental Retardation Syndrome |
MNT004 |
MR |
| Mental Retardation Syndrome, X-linked, Armfield Type |
MNT097 |
|
| Mental Retardation with Language Impairment and Autistic Features |
MNT069 |
|
| Mental Retardation X-linked Syndromic 11 |
MNT034 |
SMRXS |
| Mental Retardation X-linked Syndromic 7 |
MNT035 |
MRXS7 |
| Mental Retardation-hypotonic Facies Syndrome, X-linked |
MNT061 |
|
| Mental Retardation-skeletal Dysplasia |
MNT005 |
|
| Mental Retardation, Anterior Maxillary Protrusion, and Strabismus |
MNT118 |
|
| Mental Retardation, Autosomal Dominant 1 |
MNT048 |
MRD1 |
| Mental Retardation, Autosomal Dominant 2 |
MNT106 |
|
| Mental Retardation, Autosomal Dominant 3 |
MNT115 |
|
| Mental Retardation, Autosomal Dominant 4 |
MNT120 |
|
| Mental Retardation, Autosomal Dominant 5 |
MNT049 |
MRD5 |
| Mental Retardation, Autosomal Recessive 1 |
MNT125 |
MRT1 |
| Mental Retardation, Autosomal Recessive 13 |
MNT105 |
|
| Mental Retardation, Autosomal Recessive 2a |
MNT111 |
|
| Mental Retardation, Autosomal Recessive 3 |
MNT101 |
|
| Mental Retardation, Autosomal Recessive 5 |
MNT145 |
MRT5 |
| Mental Retardation, Autosomal Recessive 7 |
MNT051 |
|
| Mental Retardation, Autosomal Recessive, 10 |
MNT099 |
|
| Mental Retardation, Autosomal Recessive, 11 |
MNT094 |
|
| Mental Retardation, Autosomal Recessive, 12 |
MNT090 |
|
| Mental Retardation, Autosomal Recessive, 4 |
MNT100 |
|
| Mental Retardation, Autosomal Recessive, 6 |
MNT064 |
|
| Mental Retardation, Autosomal Recessive, 8 |
MNT089 |
|
| Mental Retardation, Autosomal Recessive, 9 |
MNT083 |
|
| Mental Retardation, Joint Hypermobility and Skin Laxity, with or Without Metabolic Abnormalities |
MNT067 |
|
| Mental Retardation, Nonsyndromic |
MNT052 |
MRT13 |
| Mental Retardation, Profound |
MNT072 |
|
| Mental Retardation, Severe, with Spasticity and Tapetoretinal Degeneration |
MNT078 |
|
| Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations |
MNT053 |
|
| Mental Retardation, X-linked |
MNT063 |
|
| Mental Retardation, X-linked 14 |
MNT041 |
MRX14 |
| Mental Retardation, X-linked 17/31, Microduplication |
MNT073 |
|
| Mental Retardation, X-linked 20 |
MNT076 |
|
| Mental Retardation, X-linked 23, Nonspecific |
MNT079 |
|
| Mental Retardation, X-linked 36/43/54 |
MNT066 |
|
| Mental Retardation, X-linked 52 |
MNT093 |
|
| Mental Retardation, X-linked 77 |
MNT087 |
|
| Mental Retardation, X-linked 78 |
MNT092 |
|
| Mental Retardation, X-linked 81 |
MNT088 |
|
| Mental Retardation, X-linked 82 |
MNT080 |
|
| Mental Retardation, X-linked 84 |
MNT074 |
|
| Mental Retardation, X-linked Nonspecific, 42 |
MNT095 |
|
| Mental Retardation, X-linked Nonspecific, 63 |
MNT071 |
|
| Mental Retardation, X-linked Nonspecific, Type 19 |
MNT114 |
|
| Mental Retardation, X-linked Nonspecific, Type 46 |
MNT065 |
|
| Mental Retardation, X-linked Nonspecific, Type 50 |
MNT082 |
|
| Mental Retardation, X-linked Syndromic |
MNT116 |
|
| Mental Retardation, X-linked Syndromic 16 |
MNT070 |
|
| Mental Retardation, X-linked-49 |
MNT075 |
|
| Mental Retardation, X-linked-53 |
MNT098 |
|
| Mental Retardation, X-linked-92 |
MNT110 |
|
| Mental Retardation, X-linked, 1 |
MNT077 |
|
| Mental Retardation, X-linked, 2 |
MNT085 |
|
| Mental Retardation, X-linked, 21/34 |
MNT122 |
|
| Mental Retardation, X-linked, Fraxe Type |
MNT068 |
|
| Mental Retardation, X-linked, Nonspecific |
MNT042 |
MRX21 |
| Mental Retardation, X-linked, Syndromic 12 |
MNT086 |
|
| Mental Retardation, X-linked, Syndromic 14 |
MNT055 |
|
| Mental Retardation, X-linked, Syndromic 15 (cabezas Type) |
MNT109 |
|
| Mental Retardation, X-linked, Syndromic 6, with Gynecomastia and Obesity |
MNT113 |
|
| Mental Retardation, X-linked, Syndromic-2, with Dysmorphism and Cerebral Atrophy |
MNT124 |
|
| Mental Retardation, X-linked, Syndromic-4, with Congenital Contractures and Low Fingertip Arches |
MNT104 |
|
| Mental Retardation, X-linked, Syndromic-5, with Dandy-walker Malformation, Basal Ganglia Disease, and Seizures |
MNT091 |
|
| Mental Retardation, X-linked, Syndromic, Turner Type |
MNT058 |
MRXST |
| Mental Retardation, X-linked, with Isolated Growth Hormone Deficiency |
MNT119 |
|
| Mental Retardation, X-linked, with or Without Epilepsy |
MNT117 |
|
| Mental Retardation, X-linked, with Short Stature |
MNT084 |
|
| Mephenytoin Poor Metabolizer |
MPH001 |
|
| Mercury Poisoning |
MRC003 |
|
| Merkel Cell Carcinoma |
MRK001 |
|
| Merkel Cell Carcinoma, Somatic |
MRK004 |
|
| Merrf Syndrome |
MRR001 |
MERRF |
| Merrf/melas Overlap Syndrome |
MRR006 |
|
| Mesangial Proliferative Glomerulonephritis |
MSN001 |
|
| Mesangial Sclerosis |
MSN007 |
|
| Mesenchymal Chondrosarcoma |
MSN005 |
|
| Mesenchymoma |
MSN006 |
|
| Mesenteric Lymphadenitis |
MSN002 |
|
| Mesenteric Vascular Occlusion |
MSN003 |
|
| Mesoblastic Nephroma |
MSB002 |
|
| Mesomelia |
MSM003 |
|
| Mesomelia-synostoses Syndrome |
MSM004 |
|
| Mesomelic Dysplasia |
MSM002 |
|
| Mesomelic Dysplasia Kantaputra Type |
MSM007 |
MDK |
| Metabolic Disorders |
MTB002 |
|
| Metabolic Syndrome X |
MTB001 |
AOMS1 |
| Metabolic Syndrome, Protection Against |
MTB003 |
|
| Metacarpals 4 and 5 Fusion |
MTC017 |
|
| Metachondromatosis |
MTC018 |
|
| Metachromatic Leukodystrophy |
MTC003 |
MLD |
| Metachromatic Leukodystrophy Due to Sap-b Deficiency |
MTC067 |
|
| Metanephric Adenoma |
MTN001 |
|
| Metaphyseal Anadysplasia |
MTP005 |
MAD |
| Metaphyseal Anadysplasia 1 |
MTP013 |
|
| Metaphyseal Anadysplasia 2 |
MTP014 |
|
| Metaphyseal Chondrodysplasia |
MTP002 |
|
| Metaphyseal Dysplasia |
MTP001 |
|
| Metaphyseal Dysplasia Without Hypotrichosis |
MTP003 |
CHHV |
| Metastasis Efficiency |
MTS002 |
|
| Metastasis Efficiency, Modification of |
MTS006 |
|
| Metastatic Insulinoma |
MTS004 |
|
| Metatropic Dysplasia |
MTT002 |
|
| Methemoglobinemia |
MTH007 |
|
| Methemoglobinemia, Type I |
MTH037 |
|
| Methemoglobinemia, Type Ii |
MTH038 |
|
| Methemoglobinemia, Type Iv |
MTH036 |
|
| Methemoglobinemias, Alpha- |
MTH030 |
|
| Methemoglobinemias, Beta- |
MTH031 |
|
| Methionine Adenosyltransferase Deficiency |
MTH011 |
|
| Methionine Adenosyltransferase Deficiency, Autosomal Recessive |
MTH029 |
|
| Methylcobalamin Deficiency |
MTH012 |
|
| Methylmalonate Semialdehyde Dehydrogenase Deficiency |
MTH013 |
|
| Methylmalonic Acidemia |
MTH008 |
MMA |
| Methylmalonic Acidemia with Homocystinuria |
MTH021 |
|
| Methylmalonic Aciduria and Homocystinuria |
MTH014 |
|
| Methylmalonic Aciduria and Homocystinuria Type Cblc |
MTH004 |
|
| Methylmalonic Aciduria and Homocystinuria Type Cbld |
MTH006 |
|
| Methylmalonic Aciduria and Homocystinuria Type Cblf |
MTH005 |
|
| Methylmalonic Aciduria Due to Transcobalamin Receptor Defect |
MTH032 |
|
| Methylmalonic Aciduria, Cbld Type, Variant 2 |
MTH035 |
|
| Methylmalonic Aciduria, Mut(0) Type |
MTH039 |
|
| Methylmalonyl-coenzyme a Mutase Deficiency |
MTH025 |
|
| Mevalonic Aciduria |
MVL001 |
|
| Mhc Class I Deficiency |
MHC002 |
BLSI |
| Mhc Class Ii Deficiency |
MHC001 |
BLS 2 |
| Mhc Class Ii Deficiency, Complementation Group B |
MHC003 |
|
| Michels Syndrome |
MCH010 |
|
| Micochondrial Phosphate Carrier Deficiency |
MCC009 |
|
| Micro Syndrome |
MCR029 |
|
| Microcephalic Osteodysplastic Primordial Dwarfism Type 1 |
MCR043 |
TALS |
| Microcephalic Osteodysplastic Primordial Dwarfism Type 2 |
MCR044 |
MOPD2 |
| Microcephaly |
MCR010 |
|
| Microcephaly and Digital Abnormalities with Normal Intelligence |
MCR138 |
|
| Microcephaly with Digital Anomalies |
MCR131 |
|
| Microcephaly, Cortical Malformations, and Mental Retardation |
MCR098 |
|
| Microcephaly, Mental Retardation, and Distinctive Facies, with Cardiac and Genitourinary Malformations |
MCR118 |
|
| Microcephaly, Postnatal Progressive, with Seizures and Brain Atrophy |
MCR123 |
|
| Microcephaly, Primary Autosomal Recessive, 5, with or Without Simplified Gyral Pattern |
MCR111 |
|
| Microcephaly, Seizures, and Developmental Delay |
MCR064 |
MCSZ |
| Microcoria |
MCR023 |
|
| Microcoria, Congenital |
MCR067 |
MCOR |
| Microcornea, Rod-cone Dystrophy, Cataract, and Posterior Staphyloma |
MCR106 |
|
| Microcystic Adenoma |
MCR014 |
|
| Microcystic Meningioma |
MCR001 |
|
| Microcytic Anemia |
MCR018 |
|
| Microglandular Adenosis |
MCR019 |
|
| Microhydranencephaly |
MCR025 |
MHAC |
| Micropenis |
MCR026 |
|
| Microphthalmia |
MCR013 |
|
| Microphthalmia Cataract |
MCR076 |
|
| Microphthalmia Syndromic 3 |
MCR080 |
|
| Microphthalmia Syndromic 4 |
MCR081 |
|
| Microphthalmia Syndromic 5 |
MCR082 |
|
| Microphthalmia Syndromic 6 |
MCR083 |
|
| Microphthalmia Syndromic 7 |
MCR084 |
|
| Microphthalmia Syndromic 8 |
MCR085 |
MMEP |
| Microphthalmia Syndromic 9 |
MCR086 |
|
| Microphthalmia with Cataract 1 |
MCR121 |
|
| Microphthalmia with Cataract 2 |
MCR132 |
|
| Microphthalmia with Cataract 4 |
MCR126 |
|
| Microphthalmia with Coloboma 1 |
MCR116 |
|
| Microphthalmia with Coloboma 2 |
MCR117 |
|
| Microphthalmia with Coloboma 3 |
MCR136 |
|
| Microphthalmia with Coloboma 5 |
MCR127 |
|
| Microphthalmia with Coloboma 6 |
MCR107 |
|
| Microphthalmia with Coloboma 6, Digenic |
MCR110 |
|
| Microphthalmia with Linear Skin Defects |
MCR028 |
|
| Microphthalmia, Isolated 1 |
MCR124 |
|
| Microphthalmia, Isolated 2 |
MCR137 |
|
| Microphthalmia, Isolated 3 |
MCR114 |
|
| Microphthalmia, Isolated 4 |
MCR109 |
|
| Microphthalmia, Isolated 7 |
MCR108 |
|
| Microscopic Polyangiitis |
MCR088 |
|
| Microsporidiosis |
MCR020 |
|
| Microtia |
MCR103 |
|
| 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 |
|
| Microvillus Inclusion Disease |
MCR094 |
|
| Middle Cerebral Artery Infarction |
MDD003 |
|
| Middle Ear Cancer |
MDD012 |
|
| Middle Ear Carcinoma |
MDD009 |
|
| Middle Ear Cholesteatoma |
MDD002 |
|
| Middle Ear Disease |
MDD010 |
|
| Middle Lobe Syndrome |
MDD005 |
|
| Migraine |
MGR002 |
|
| Migraine with Aura |
MGR003 |
|
| Migraine Without Aura |
MGR001 |
|
| Migraine, Familial Basilar |
MGR007 |
|
| Migraine, Resistance to |
MGR009 |
|
| Mikulicz Disease |
MKL001 |
|
| Mild Pre-eclampsia |
MLD002 |
|
| Miles-carpenter X-linked Mental Retardation Syndrome |
MLS002 |
MCS |
| Miliaria |
MLR009 |
|
| Miliaria Rubra |
MLR001 |
|
| Miliary Tuberculosis |
MLR002 |
|
| Miller Fisher Syndrome |
MLL002 |
|
| Miller-dieker Lissencephaly |
MLL003 |
|
| Miller-dieker Syndrome |
MLL005 |
MDS |
| Minicore Myopathy with External Ophthalmoplegia |
MNC011 |
|
| Mirizzi Syndrome |
MRZ001 |
|
| Mirror Movements, Congenital |
MRR007 |
|
| Mirror-image Polydactyly |
MRR004 |
|
| Mite Infestation |
MTN002 |
|
| Mitochondrial Cardiomyopathy |
MTC028 |
|
| Mitochondrial Complex I Deficiency |
MTC007 |
|
| Mitochondrial Complex Ii Deficiency |
MTC020 |
|
| Mitochondrial Complex Iii Deficiency |
MTC008 |
|
| Mitochondrial Complex V Deficiency |
MTC021 |
|
| Mitochondrial Dna Depletion Myopathy |
MTC009 |
|
| Mitochondrial Dna Depletion Syndrome |
MTC010 |
|
| Mitochondrial Dna Depletion Syndrome 1 (mngie Type) |
MTC061 |
|
| Mitochondrial Dna Depletion Syndrome 2 (myopathic Type) |
MTC062 |
|
| Mitochondrial Dna Depletion Syndrome 3 (hepatocerebral Type) |
MTC063 |
|
| Mitochondrial Dna Depletion Syndrome 5 (encephalomyopathic with Methylmalonic Aciduria) |
MTC059 |
|
| Mitochondrial Dna Depletion Syndrome 6 (hepatocerebral Type) |
MTC058 |
|
| Mitochondrial Dna Depletion Syndrome 7 (hepatocerebral Type) |
MTC054 |
|
| Mitochondrial Dna Depletion Syndrome 9 (encephalomyopathic Type with Methylmalonic Aciduria) |
MTC060 |
|
| Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form |
MTC033 |
|
| Mitochondrial Dna Depletion Syndrome, Hepatocerebral Form |
MTC034 |
|
| Mitochondrial Dna-associated Leigh Syndrome and Narp |
MTC015 |
|
| Mitochondrial Encephalomyopathy |
MTC004 |
|
| Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-like Episodes |
MTC023 |
MELAS |
| Mitochondrial Myopathy and Sideroblastic Anemia |
MTC011 |
MLASA |
| Mitochondrial Myopathy and Sideroblastic Anemia 1 |
MTC064 |
|
| Mitochondrial Myopathy with Lactic Acidosis |
MTC026 |
|
| Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome |
MTC012 |
|
| Mitochondrial Neurogastrointestinal Encephalopathy Disease |
MTC016 |
MEPOP |
| Mitochondrial Phosphate Carrier Deficiency |
MTC037 |
MPCD |
| Mitochondrial Recessive Ataxia Syndrome (includes Sando and Scae) |
MTC057 |
|
| Mitochondrial Respiratory Chain Complex Ii Deficiency |
MTC013 |
|
| Mitochondrial Trifunctional Protein Deficiency |
MTC027 |
|
| Mitral Atresia |
MTR027 |
|
| Mitral Valve Disease |
MTR012 |
|
| Mitral Valve Insufficiency |
MTR002 |
|
| Mitral Valve Prolapse |
MTR005 |
|
| Mitral Valve Prolapse, Myxomatous 1 |
MTR040 |
|
| Mitral Valve Prolapse, Myxomatous 2 |
MTR041 |
|
| Mitral Valve Prolapse, Myxomatous 3 |
MTR042 |
|
| Mitral Valve Stenosis |
MTR003 |
|
| Mixed Cell Type Cancer |
MXD023 |
|
| Mixed Connective Tissue Disease |
MXD005 |
MCTD |
| Mixed Ductal-endocrine Carcinoma |
MXD014 |
|
| Mixed Endometrial Stromal and Smooth Muscle Tumor |
MXD017 |
|
| Mixed Epithelial Stromal Tumour |
MXD010 |
|
| Mixed Germ Cell-sex Cord Neoplasm |
MXD008 |
|
| Mixed Glioma |
MXD026 |
|
| Mixed Gonadal Dysgenesis |
MXD016 |
|
| Mixed Malaria |
MXD019 |
|
| Miyoshi Muscular Dystrophy 2 |
MYS019 |
|
| Miyoshi Muscular Dystrophy 3 |
MYS014 |
MMD3 |
| Miyoshi Myopathy |
MYS006 |
MM |
| Mobius Syndrome |
MBS001 |
|
| Moebius Syndrome |
MBS002 |
|
| Moebius Syndrome-3 |
MBS004 |
|
| Mohr-tranebjaerg Syndrome |
MHR001 |
DDP |
| Molluscum Contagiosum |
MLL001 |
|
| Molybdenum Cofactor Deficiency |
MLY001 |
MOCOD |
| Molybdenum Cofactor Deficiency, Type a |
MLY003 |
|
| Molybdenum Cofactor Deficiency, Type B |
MLY004 |
|
| Molybdenum Cofactor Deficiency, Type C |
MLY002 |
|
| Mondini Dysplasia |
MND005 |
|
| Mongolian Spot |
MNG001 |
PXE |
| Monilethrix |
MNL001 |
|
| Monkeypox |
MNK002 |
|
| Monoclonal Gammopathy of Uncertain Significance |
MNC006 |
MGUS |
| Monoclonal Gammopathy of Undetermined Significance |
MNC013 |
MGUS |
| Monocytic Leukemia |
MNC007 |
|
| Monogenic Disease |
MNG002 |
|
| Monomelic Amyotrophy |
MNM001 |
|
| Mononeuritis |
MNN014 |
|
| Mononeuritis Multiplex |
MNN002 |
|
| Mononeuropathy |
MNN017 |
|
| Mononeuropathy of the Median Nerve, Mild |
MNN028 |
|
| Monophasic Synovial Sarcoma |
MNP001 |
|
| Mood Disorder |
MDD011 |
|
| Mooren's Ulcer |
MRN002 |
|
| Morbid Obesity |
MRB003 |
|
| Morgagni Cataract |
MRG001 |
|
| Morning Glory Disc Anomaly |
MRN004 |
|
| Morphine Dependence |
MRP001 |
|
| Morquio Syndrome B |
MRQ001 |
|
| Morvan's Fibrillary Chorea |
MRV001 |
|
| Mosaic Trisomy 8 |
MSC020 |
|
| Mosaic Variegated Aneuploidy Syndrome |
MSC022 |
|
| Motion Sickness |
MTN003 |
|
| Motor Neuritis |
MTR013 |
|
| Motor Neuron Disease |
MTR014 |
|
| Motor Neuronopathy |
MTR015 |
|
| Motor Neuronopathy, Distal Hereditary, with Vocal Cord Paralysis |
MTR043 |
|
| Motor Peripheral Neuropathy |
MTR007 |
HSMN |
| Mouth Disease |
MTH009 |
|
| Mowat-wilson Syndrome |
MWT001 |
MWS |
| Moyamoya Disease |
MYM002 |
|
| Mthfr Deficiency |
MTH027 |
|
| Mthfr Thermolabile Variant |
MTH028 |
|
| Mu Chain Disease |
MCH003 |
|
| Mucinous Adenocarcinoma |
MCN001 |
|
| Mucinous Adenofibroma |
MCN006 |
|
| Mucinous Cystadenocarcinoma |
MCN008 |
|
| Mucinous Ovarian Cystadenoma |
MCN003 |
|
| Mucinous Stomach Adenocarcinoma |
MCN009 |
|
| Muckle-wells Syndrome |
MCK007 |
MWS |
| Mucocutaneous Leishmaniasis |
MCC002 |
|
| Mucoepidermoid Carcinoma |
MCP006 |
MEC |
| Mucoepidermoid Salivary Gland Carcinoma |
MCP011 |
|
| Mucolipidoses |
MCL022 |
|
| Mucolipidosis |
MCL001 |
|
| Mucolipidosis Ii |
MCL015 |
ICD |
| Mucolipidosis Iii Gamma |
MCL016 |
|
| Mucolipidosis Iiia |
MCL011 |
ML3 |
| Mucolipidosis Iiic |
MCL012 |
|
| Mucolipidosis Iv |
MCL013 |
ML4 |
| Mucopolysaccharidisis Type Iiia (sanfilippo a) |
MCP027 |
|
| Mucopolysaccharidosis |
MCP010 |
MPS |
| Mucopolysaccharidosis I |
MCP002 |
MPS1 |
| Mucopolysaccharidosis Ih |
MCP012 |
|
| Mucopolysaccharidosis Ii |
MCP009 |
MPS 2 |
| Mucopolysaccharidosis Iii |
MCP001 |
|
| Mucopolysaccharidosis Iv |
MCP004 |
|
| Mucopolysaccharidosis Type Iiib (sanfilippo B) |
MCP026 |
|
| Mucopolysaccharidosis Type Iiic |
MCP020 |
|
| Mucopolysaccharidosis Type Iiic (sanfilippo C) |
MCP025 |
|
| Mucopolysaccharidosis Type Iiid |
MCP014 |
|
| Mucopolysaccharidosis Type Ivb (morquio) |
MCP023 |
|
| Mucopolysaccharidosis Type Ix |
MCP015 |
MPS9 |
| Mucopolysaccharidosis Type Vi (maroteaux-lamy) |
MCP024 |
|
| Mucopolysaccharidosis Vi |
MCP005 |
MPS6 |
| Mucopolysaccharidosis Vii |
MCP003 |
SLS |
| Muenke Syndrome |
MNK003 |
|
| Muir-torre Syndrome |
MRT001 |
|
| Mulibrey Nanism |
MLB001 |
|
| Mullerian Aplasia |
MLL009 |
|
| Mullerian Aplasia and Hyperandrogenism |
MLL011 |
|
| Multicentric Carpotarsal Osteolysis Syndrome |
MLT092 |
MCTO |
| Multicentric Osteolysis Nephropathy |
MLT033 |
|
| Multicentric Reticulohistiocytosis |
MLT016 |
|
| Multidrug-resistant Tuberculosis |
MLT006 |
|
| Multifocal Choroiditis |
MLT035 |
|
| Multifocal Fibrosclerosis |
MLT036 |
|
| Multifocal Motor Neuropathy |
MLT075 |
|
| Multifocal Osteogenic Sarcoma |
MLT017 |
|
| Multilocular Clear Cell Renal Cell Carcinoma |
MLT003 |
|
| Multiminicore Disease |
MLT028 |
MMD |
| Multinodular Goiter |
MLT008 |
|
| Multiple Carboxylase Deficiency |
MLT018 |
|
| Multiple Chemical Sensitivity |
MLT001 |
|
| Multiple Cranial Nerve Palsy |
MLT009 |
|
| Multiple Cutaneous and Mucosal Venous Malformations |
MLT029 |
VMCM |
| Multiple Cutaneous and Uterine Leiomyomas |
MLT066 |
MCUL |
| Multiple Cutaneous and Uterine Leiomyomata |
MLT023 |
|
| Multiple Endocrine Neoplasia |
MLT074 |
MEA |
| Multiple Endocrine Neoplasia Iia |
MLT024 |
|
| Multiple Endocrine Neoplasia Iib |
MLT025 |
|
| Multiple Endocrine Neoplasia Type 2a |
MLT042 |
|
| Multiple Endocrine Neoplasia Type 4 |
MLT067 |
MEN4 |
| Multiple Epiphyseal Dysplasia |
MLT007 |
EDM |
| Multiple Epiphyseal Dysplasia, Dominant |
MLT030 |
|
| Multiple Epiphyseal Dysplasia, Recessive |
MLT031 |
EDM4 |
| Multiple Familial Trichoepithelioma |
MLT048 |
EAC |
| Multiple Intestinal Atresia |
MLT015 |
|
| Multiple Meningiomas |
MLT085 |
|
| Multiple Mitochondrial Dysfunctions Syndrome |
MLT027 |
|
| Multiple Mitochondrial Dysfunctions Syndrome 1 |
MLT068 |
MMDS1 |
| Multiple Mitochondrial Dysfunctions Syndrome 2 |
MLT069 |
MMDS2 |
| Multiple Myeloma |
MLT019 |
|
| Multiple Myeloma, Resistance to |
MLT079 |
|
| Multiple Pterygium Syndrome Lethal Type |
MLT055 |
LMPS |
| Multiple Sclerosis |
MLT020 |
MS |
| Multiple Sclerosis, Disease Progression, Modifier of |
MLT077 |
|
| Multiple Self Healing Squamous Epithelioma |
MLT058 |
ESS1 |
| Multiple Symmetric Lipomatosis |
MLT012 |
|
| Multiple Symmetrical Lipomatosis |
MLT002 |
|
| Multiple Synostoses Syndrome 2 |
MLT060 |
SYNS2 |
| Multiple Synostoses Syndrome 3 |
MLT078 |
|
| Multiple System Atrophy |
MLT021 |
MSA |
| Multisystemic Smooth Muscle Dysfunction Syndrome |
MLT073 |
|
| Mumps |
MMP001 |
|
| Munchausen by Proxy |
MNC002 |
|
| Mungen Syndrome |
MNG005 |
|
| Murcs Association |
MRC004 |
|
| Murray Valley Encephalitis |
MRR003 |
|
| Muscle Disorders |
MSC033 |
|
| Muscle Glycogenosis |
MSC006 |
|
| Muscle Hypertrophy |
MSC007 |
|
| Muscle Phosphorylase Kinase Deficiency |
MSC032 |
|
| Muscle Strength Quantitative Trait Locus 1 |
MSC054 |
|
| Muscle-eye-brain Disease |
MSC008 |
MEB |
| Muscular Atrophy |
MSC003 |
|
| Muscular Dystrophy |
MSC005 |
|
| Muscular Dystrophy with Epidermolysis Bullosa Simplex |
MSC009 |
|
| Muscular Dystrophy with Rimmed Vacuoles |
MSC010 |
|
| Muscular Dystrophy-dystroglycanopathy |
MSC002 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital with Brain and Eye Anomalies), Type a, 1 |
MSC047 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital with Brain and Eye Anomalies), Type a, 2 |
MSC043 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital with Brain and Eye Anomalies), Type a, 4 |
MSC037 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital with Brain and Eye Anomalies), Type a, 5 |
MSC034 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital with Brain and Eye Anomalies), Type a, 6 |
MSC041 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital with Mental Retardation), Type B, 1 |
MSC048 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital with Mental Retardation), Type B, 2 |
MSC044 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital with Mental Retardation), Type B, 6 |
MSC042 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital with or Without Mental Retardation), Type B, 5 |
MSC035 |
|
| Muscular Dystrophy-dystroglycanopathy (congenital Without Mental Retardation), Type B, 4 |
MSC038 |
|
| Muscular Dystrophy-dystroglycanopathy (limb-girdle), Type C, 5 |
MSC036 |
|
| Muscular Dystrophy, Congenital, 1b |
MSC050 |
|
| Muscular Dystrophy, Congenital, Merosin-positive |
MSC029 |
|
| Muscular Dystrophy, Duchenne and Becker Type |
MSC012 |
DBMD |
| Muscular Dystrophy, Duchenne and Becker Types |
MSC011 |
DBMD |
| Muscular Dystrophy, Limb-girdle, Type Ic |
MSC049 |
|
| Mushroom Workers' Lung |
MSH001 |
|
| Musical Aptitude Qtl 1 |
MSC053 |
|
| Musk-related Congenital Myasthenic Syndrome |
MSK001 |
|
| Mutagen Sensitivity |
MTG002 |
|
| Mutism |
MTS001 |
|
| Mutyh-associated Polyposis |
MTY001 |
|
| Myasthenia |
MYS008 |
|
| Myasthenia Gravis |
MYS003 |
MG |
| Myasthenia Gravis with Thymus Hyperplasia |
MYS007 |
|
| Myasthenia Gravis, Neonatal Transient |
MYS023 |
|
| Myasthenia, Familial Infantile, 1 |
MYS018 |
|
| Myasthenia, Limb-girdle, Familial |
MYS017 |
|
| Myasthenic Syndrome |
MYS009 |
|
| Myasthenic Syndrome, Congenital, Associated with Facial Dysmorphism and Acetylcholine Receptor Deficiency |
MYS020 |
|
| Myasthenic Syndrome, Fast-channel Congenital |
MYS022 |
|
| Mycetoma |
MYC012 |
|
| Mycobacterial and Salmonella Infections |
MYC057 |
|
| Mycobacterial Infection |
MYC009 |
|
| Mycobacterium Abscessus |
MYC013 |
|
| Mycobacterium Avium Complex Disease |
MYC002 |
MAC |
| Mycobacterium Chelonae |
MYC014 |
|
| Mycobacterium Fortuitum |
MYC015 |
|
| Mycobacterium Gordonae |
MYC016 |
|
| Mycobacterium Kansasii |
MYC017 |
|
| Mycobacterium Malmoense |
MYC018 |
|
| Mycobacterium Marinum |
MYC019 |
|
| Mycobacterium Tuberculosis |
MYC056 |
|
| Mycobacterium Tuberculosis Infection, Protection Against |
MYC044 |
|
| Mycobacterium Tuberculosis, Protection Against |
MYC041 |
|
| Mycobacterium Tuberculosis, Susceptibility to Infection by |
MYC020 |
|
| Mycosis Fungoides |
MYC006 |
MF |
| Myelitis |
MYL001 |
|
| Myelodysplasia Syndrome |
MYL008 |
|
| Myelodysplastic Myeloproliferative Cancer |
MYL004 |
|
| Myelodysplastic Syndrome |
MYL009 |
MDS |
| Myelodysplastic Syndrome, Preleukemic |
MYL029 |
|
| Myelofibrosis |
MYL005 |
|
| Myeloid Leukemia |
MYL006 |
|
| Myeloid Malignancy |
MYL010 |
|
| Myeloid Malignancy, Predisposition to |
MYL028 |
|
| Myeloid Sarcoma |
MYL003 |
|
| Myelokathexis |
MYL011 |
|
| Myelokathexis, Isolated |
MYL026 |
|
| Myeloma |
MYL007 |
|
| Myelomeningocele |
MYL020 |
|
| Myelomonocytic Leukemia |
MYL012 |
|
| Myeloperoxidase Deficiency |
MYL013 |
|
| Myeloproliferative Disorder |
MYL014 |
|
| Myeloproliferative Disorder with Eosinophilia |
MYL015 |
|
| Myeloproliferative Disorder with Erythrocytosis |
MYL027 |
|
| Myiasis |
MYS004 |
|
| Myoadenylate Deaminase Deficiency |
MYD001 |
MADA |
| Myoblastoma |
MYB001 |
|
| Myocardial Infarcation |
MYC059 |
|
| Myocardial Infarction |
MYC007 |
|
| Myocardial Infarction 2 |
MYC058 |
|
| Myocardial Infarction Susceptibility |
MYC035 |
|
| Myocardial Stunning |
MYC005 |
|
| Myocarditis |
MYC008 |
|
| Myoclonic Astatic Epilepsy |
MYC023 |
|
| Myoclonic Cerebellar Dyssynergia |
MYC001 |
|
| Myoclonic Epilepsy, Juvenile, 4 |
MYC037 |
|
| Myoclonus |
MYC033 |
|
| Myoclonus Epilepsy |
MYC026 |
|
| Myoclonus-dystonia |
MYC011 |
DYT11 |
| Myoepithelial Carcinoma |
MYP002 |
|
| Myoepithelioma |
MYP001 |
|
| Myofascial Pain Syndrome |
MYF002 |
|
| Myofibrillar Myopathy |
MYF003 |
|
| Myofibroma |
MYF001 |
|
| Myoglobinuria Recurrent |
MYG003 |
|
| Myoglobinuria, Acute Recurrent, Autosomal Recessive |
MYG004 |
|
| Myokymia |
MYK002 |
|
| Myokymia with Neonatal Epilepsy |
MYK001 |
|
| Myoma |
MYM001 |
MYOMA |
| Myopathy |
MYP004 |
|
| Myopathy Congenital |
MYP011 |
|
| Myopathy Due to Cpt Ii Deficiency |
MYP007 |
|
| Myopathy of Critical Illness |
MYP003 |
|
| Myopathy with Deficiency of Iscu |
MYP009 |
|
| Myopathy, Actin, Congenital, with Cores |
MYP029 |
|
| Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
MYP028 |
|
| Myopathy, Cardioskeletal, Desmin-related, with Cataract |
MYP036 |
|
| Myopathy, Congenital, with Fiber-type Disproportion 1 |
MYP030 |
|
| Myopathy, Congenital, with Fiber-type Disproportion, X-linked |
MYP039 |
|
| Myopathy, Desmin-related, Cardioskeletal |
MYP037 |
|
| Myopathy, Distal 3 |
MYP032 |
|
| Myopathy, Distal, with Anterior Tibial Onset |
MYP035 |
|
| Myopathy, Distal, with Decreased Caveolin 3 |
MYP034 |
|
| Myopathy, Early-onset, Areflexia, Respiratory Distress, and Dysphagia |
MYP020 |
|
| Myopathy, Hyaline Body |
MYP033 |
|
| Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2 |
MYP022 |
|
| Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay |
MYP017 |
|
| Myopathy, Myofibrillar, Filamin C-related |
MYP027 |
|
| Myopathy, Myofibrillar, Zasp-related |
MYP031 |
|
| Myopia |
MYP006 |
|
| Myopia 10 |
MYP044 |
|
| Myopia 11 |
MYP053 |
|
| Myopia 12 |
MYP045 |
|
| Myopia 13 |
MYP046 |
|
| Myopia 15 |
MYP043 |
|
| Myopia 16 |
MYP052 |
|
| Myopia 17 |
MYP042 |
|
| Myopia 5 |
MYP049 |
|
| Myopia 6 |
MYP018 |
MYP6 |
| Myopia 7 |
MYP040 |
|
| Myopia 8 |
MYP041 |
|
| Myopia 9 |
MYP048 |
|
| Myopia-1 |
MYP047 |
|
| Myopia-2 |
MYP051 |
|
| Myopia-3 |
MYP050 |
|
| Myosclerosis, Autosomal Recessive |
MYS016 |
|
| Myosclerosis, Congenital |
MYS021 |
|
| Myositis |
MYS005 |
|
| Myositis Fibrosa |
MYS002 |
|
| Myositis Ossificans |
MYS001 |
|
| Myostatin-related Muscle Hypertrophy |
MYS010 |
|
| Myotilinopathy |
MYT004 |
|
| Myotonia |
MYT011 |
|
| Myotonia Congenita Autosomal Recessive |
MYT009 |
|
| Myotonia Congenita, Atypical, Acetazolamide-responsive |
MYT015 |
|
| Myotonia Congenita, Dominant |
MYT013 |
|
| Myotonia Congenita, Recessive |
MYT012 |
|
| Myotonia Levior |
MYT005 |
|
| Myotonia Levior, Recessive |
MYT014 |
|
| Myotonic Dystrophy |
MYT002 |
|
| Myotonic Dystrophy Type 1 |
MYT006 |
DM1 |
| Myotonic Dystrophy Type 2 |
MYT007 |
DM2 |
| Myringitis Bullosa Hemorrhagica |
MYR001 |
|
| Myxedema |
MYX004 |
|
| Myxoid Chondrosarcoma |
MYX008 |
|
| Myxoid Leiomyosarcoma |
MYX006 |
|
| Myxoid Liposarcoma |
MYX005 |
|
| Myxoma |
MYX009 |
|
| Myxopapillary Ependymoma |
MYX001 |
|
