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Mac Ardle disease   |   Mac Dermot Patton Williams syndrome   |   Mac Dermot Winter syndrome   |   Machado-Joseph Disease   |   Macias Flores Garcia Cruz Rivera syndrome   |   Mackay Shek Carr syndrome   |   Macleod Fraser syndrome   |   Macrocephaly cutis marmorata telangiectatica   |   Macrocephaly dominant type   |   Macrocephaly mental retardation facial dysmorphism   |   Macrocephaly mesodermal hamartoma spectrum   |   Macrocephaly mesomelic arms talipes   |   Macrocephaly pigmentation large hands feet   |   Macrocephaly short stature paraplegia   |   Macrodactyly of the foot   |   Macrodactyly of the hand   |   Macroepiphyseal dysplasia Mcalister Coe type   |   Macroglobulinemia   |   Macroglossia   |   Macroglossia dominant   |   Macroglossia exomphalos gigantism   |   Macrogyria pseudobulbar palsy   |   Macrophagic myofasciitis   |   Macrosomia developmental delay dysmorphism   |   Macrosomia microphthalmia cleft palate   |   Macrothrombocytopenia progressive deafness   |   Macrothrombocytopenia with leukocyte inclusions   |   Macular corneal dystrophy   |   Macular Degeneration   |   Macular degeneration juvenile   |   Macular degeneration, age-related   |   Macular degeneration, polymorphic   |   Macular dystrophy, vitelliform   |   Macules hereditary congenital hypopigmented and hyperpigmented   |   Mad cow disease   |   Madelung's Disease   |   Madokoro Ohdo Sonoda syndrome   |   Maffucci Syndrome   |   Mageirocophobia   |   Maghazaji syndrome   |   Magnesium defect in renal tubular transport of   |   Magnesium wasting renal   |   Mal de Debarquement   |   Malakoplakia   |   Malaria   |   Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency   |   Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency   |   Male pseudohermaphroditism due to defective LH molecule   |   Malformations in neuronal migration   |   Malignant astrocytoma   |   Malignant fibrous histiocytoma   |   Malignant germ cell tumor   |   Malignant Hyperthermia   |   Malignant hyperthermia arthrogryposis torticollis   |   Malignant hyperthermia susceptibility type 1   |   Malignant hyperthermia susceptibility type 2   |   Malignant hyperthermia susceptibility type 3   |   Malignant hyperthermia susceptibility type 4   |   Malignant hyperthermia susceptibility type 5   |   Malignant hyperthermia susceptibility type 6   |   Malignant mesenchymal tumor   |   Malignant mixed Mullerian tumor   |   Malignant paroxysmal ventricular tachycardia   |   Mallory Weiss Syndrome   |   Malonic aciduria   |   Malonyl-CoA decarboxylase deficiency   |   Malouf syndrome   |   Malpuech facial clefting syndrome   |   Mandibuloacral dysplasia   |   Mandibulofacial dysostosis deafness postaxial polydactly   |   Manic Depression, Bipolar   |   Manic-depressive psychosis, genetic types   |   Mannosidosis   |   Manouvrier syndrome   |   Mansonelliasis   |   Mantle Cell Lymphoma   |   Maple Syrup Urine Disease   |   Marashi Gorlin syndrome   |   Marburg fever   |   Marchiafava Bignami disease   |   Marchiafava-Micheli disease   |   Marcus Gunn Phenomenon   |   Marden Walker like syndrome   |   Marden Walker Syndrome   |   Marek disease   |   Marfan Syndrome   |   Marfan Syndrome type II   |   Marfan Syndrome type III   |   Marfan Syndrome type IV   |   Marfan Syndrome type V   |   Marfan-Like syndrome   |   Marfan-like syndrome, Boileau type   |   Marfanoid craniosynostosis syndrome   |   Marfanoid hypermobility   |   Marfanoid mental retardation syndrome autosomal   |   Marginal glioneuronal heterotopia   |   Marie type ataxia   |   Marie Unna congenital hypotrichosis   |   Marinesco Sjogren like syndrome   |   Marinesco Sjogren Syndrome   |   Marion Mayers syndrome   |   Markel Vikkula Mulliken syndrome   |   Marles Greenberg Persaud syndrome   |   Maroteaux Cohen Solal Bonaventure syndrome   |   Maroteaux Fonfria syndrome   |   Maroteaux Lamy Syndrome   |   Maroteaux Le Merrer Bensahel syndrome   |   Maroteaux Stanescu Cousin syndrome   |   Maroteaux Verloes Stanescu syndrome   |   Maroteaux-Lamy syndrome   |   Marphanoid syndrome type De Silva   |   Marsden Nyhan Sakati syndrome   |   Marsden syndrome   |   Marshall Smith Syndrome   |   Marshall Syndrome   |   Marshall-Smith syndrome   |   Martinez Monasterio Pinheiro syndrome   |   Martsolf Reed Hunter syndrome   |   Martsolf syndrome   |   MASA syndrome   |   Mass syndrome   |   Massa Casaer Ceulemans syndrome   |   Mast cell disease   |   Mastigophobia   |   Mastocytosis   |   Mastocytosis, short stature, hearing loss   |   Mastoiditis   |   Mastroiacovo De Rosa Satta syndrome   |   Mastroiacovo Gambi Segni syndrome   |   MAT deficiency   |   Maternal hyperphenylalaninemia   |   Maternally inherited diabetes and deafness   |   Mathieu De Broca Bony syndrome   |   Matsoukas Liarikos Giannika syndrome   |   Matthew-Wood syndrome   |   Maturity onset diabetes of the young   |   Maumenee syndrome   |   Maxillary double lip   |   Maxillofacial Dysostosis   |   Maxillonasal Dysplasia, Binder Type   |   May Hegglin Anomaly   |   Mayer Rokitanski Kuster syndrome   |   McAlister Crane syndrome   |   McArdle disease   |   McCallum Macadam Johnston syndrome   |   McCune Albright Syndrome   |   McDonough syndrome   |   McDowall syndrome   |   McGillivray syndrome   |   McKusick Kaufman syndrome   |   McKusick Type Metaphyseal Chondrodysplasia   |   McLain Debakian syndrome   |   McPherson Clemens syndrome   |   McPherson Robertson Cammarano syndrome   |   Meacham Winn Culler syndrome   |   Meadows syndrome   |   Measles   |   Meckel like syndrome   |   Meckel Syndrome   |   Medeira Dennis Donnai syndrome   |   Median cleft lip corpus callosum lipoma skin polyps   |   Median nodule of the upper lip   |   Mediastinal endodermal sinus tumors   |   Mediterranean fever   |   Mediterranean Fever, Familial   |   Medium Chain Acyl CoA Dehydrogenase Deficiency   |   Medrano Roldan syndrome   |   Medullary Cystic Kidney Disease/Nephronophthisis   |   Medullary Sponge Kidney   |   Medullary thyroid carcinoma   |   Medulloblastoma   |   Megacystis microcolon intestinal hypoperistalsis syndrome   |   Megaduodenum   |   Megaepiphyseal dwarfism   |   Megalencephalic leukodystrophy   |   Megalencephaly-cystic leukodystrophy   |   Megaloblastic anemia   |   Megalocornea Mental Retardation Syndrome   |   Megalocytic Interstitial Nephritis   |   Mehes syndrome   |   Mehta Lewis Patton syndrome   |   Meier Blumberg Imahorn syndrome   |   Meier Rotschild syndrome   |   Meige Syndrome   |   Meigel disease   |   Meinecke Pepper syndrome   |   Meinecke syndrome   |   Melanoma type 1   |   Melanoma type 2   |   Melanoma, familial   |   Melanoma, Malignant   |   Melanoma-astrocytoma syndrome   |   Melanosis neurocutaneous   |   MELAS Syndrome   |   Meleda Disease   |   Melhem Fahl syndrome   |   Melioidosis   |   Melkersson Rosenthal Syndrome   |   Melnick Needles Syndrome   |   Melnick-Needles osteodysplasty   |   Melnick-Needles syndrome   |   Melophobia   |   Membranoproliferative Glomerulonephritis Type II   |   Mendelian susceptibility to atypical mycobacteria   |   Menetrier's disease   |   Mengel Konigsmark syndrome   |   Meniere Disease   |   Meningeal angiomatosis cleft hypoplastic left heart   |   Meningioma   |   Meningioma 1   |   Meningitis   |   Meningitis, Bacterial   |   Meningitis, Meningococcal   |   Meningitis, Tuberculous   |   Meningocele   |   Meningococcemia   |   Meningoencephalocele   |   Meningoencephalocele-arthrogryposis-hypoplastic thumb   |   Meningomyelocele   |   Menkes Disease   |   Menophobia   |   Mental deficiency-epilepsy-endocrine disorders   |   Mental mixed retardation deafnes clubbed digits   |   Mental retardation   |   Mental retardation anophthalmia craniosynostosis   |   Mental retardation arachnodactyly hypotonia telangiectasia   |   Mental retardation athetosis microphthalmia   |   Mental retardation blepharophimosis obesity web neck   |   Mental retardation Buenos Aires type   |   Mental retardation cataracts calcified pinnae myopathy   |   Mental retardation coloboma slimness   |   Mental retardation contractural arachnodactyly   |   Mental retardation dysmorphism hypogonadism diabetes   |   Mental retardation epilepsy   |   Mental retardation epilepsy bulbous nose   |   Mental retardation gynecomastia obesity X linked   |   Mental retardation hip luxation G6PD variant   |   Mental retardation hypocupremia hypobetalipoproteinemia   |   Mental retardation hypotonia skin hyperpigmentation   |   Mental retardation macrocephaly coarse facies hypotonia   |   Mental retardation microcephaly phalangeal facial   |   Mental retardation microcephaly unusual facies   |   Mental retardation Mietens Weber type   |   Mental retardation multiple nevi   |   Mental retardation myopathy short stature endocrine defect   |   Mental retardation nasal hypoplasia obesity genital hypoplasia   |   Mental retardation nasal papillomata   |   Mental retardation osteosclerosis   |   Mental retardation progressive spasticity   |   Mental retardation psychosis macroorchidism   |   Mental retardation short broad thumbs   |   Mental retardation short stature absent phalanges   |   Mental retardation short stature Bombay phenotype   |   Mental retardation short stature cleft palate unusual facies   |   Mental retardation short stature deafness genital   |   Mental retardation short stature hand contractures genital anomalies   |   Mental retardation short stature heart and skeletal anomalies   |   Mental retardation short stature hypertelorism   |   Mental retardation short stature microcephaly eye   |   Mental retardation short stature ocular and articular anomalies   |   Mental retardation short stature scoliosis   |   Mental retardation short stature unusual facies   |   Mental retardation short stature wedge shaped epiphyses   |   Mental retardation skeletal dysplasia abducens palsy   |   Mental retardation Smith Fineman Myers type   |   Mental retardation spasticity ectrodactyly   |   Mental retardation unusual facies   |   Mental retardation unusual facies Ampola type   |   Mental retardation unusual facies Davis Lafer type   |   Mental retardation unusual facies talipes hand anomalies   |   Mental retardation Wolff type   |   Mental retardation X linked Atkin type   |   Mental retardation X linked borderline Maoa metabolism anomaly   |   Mental retardation X linked Brunner type   |   Mental retardation X linked dysmorphism   |   Mental retardation X linked dystonia dysarthria   |   Mental retardation X linked severe Gustavson type   |   Mental retardation X linked short stature obesity   |   Mental retardation X linked Tranebjaerg type seizures psoriasis   |   Mental retardation, unexplained   |   Mental retardation, X linked, Marfanoid habitus   |   Mental retardation, X linked, nonspecific   |   Mental retardation, X-linked 14   |   Mental retardation-polydactyly-uncombable hair   |   Mercury poisoning   |   Meretoja syndrome   |   Merkle tumors   |   Merlob Grunebaum Reisner syndrome   |   Merlob syndrome   |   MERRF Syndrome   |   Mesangial sclerosis, diffuse   |   Mesenteric ischemia   |   Mesenteric panniculitis   |   Mesenteritis, Retractile   |   Mesodermal defects lower type   |   Mesomelia   |   Mesomelia synostoses   |   Mesomelic dwarfism cleft palate camptodactyly   |   Mesomelic dwarfism Langer type   |   Mesomelic dwarfism Nievergelt type   |   Mesomelic dwarfism Reinhardt Pfeiffer type   |   Mesomelic dysplasia skin dimples   |   Mesomelic dysplasia Thai type   |   Mesomelic syndrome Pfeiffer type   |   Mesothelioma   |   Metabolic acidosis   |   Metabolic disorder   |   Metabolic Syndrome X   |   Metacarpals 4 and 5 fusion   |   Metachondromatosis   |   Metageria   |   Metaphyseal anadysplasia   |   Metaphyseal chondrodysplasia Spahr type   |   Metaphyseal chondrodysplasia, others   |   Metaphyseal Chondrodysplasia, Schmid Type   |   Metaphyseal dysostosis mental retardation conductive deafness   |   Metaphyseal dysplasia maxillary hypoplasia brachydactyly   |   Metaphyseal dysplasia Pyle type   |   Metastatic insulinoma   |   Metatarsus adductus   |   Metathesiophobia   |   Metatrophic dysplasia   |   Metatropic dwarfism   |   Metatropic Dysplasia I   |   Methimazole antenatal infection   |   Methionine adenosyl transferase deficiency   |   Methyl mercury antenatal infection   |   Methylcobalamin deficiency cbl G type   |   Methylcobalamin deficiency, cbl E complementation type   |   Methylenetetrahydrofolate reductase deficiency   |   Methylmalonic acidemia   |   Methylmalonic acidemia with homocystinuria   |   Methylmalonic aciduria microcephaly cataract   |   Methylmalonicacidemia with homocystinuria, cbl D   |   Methylmalonicaciduria with homocystinuria, cbl F   |   Methylmalonicaciduria, vitamin B12 unresponsive, mut-0   |   Methylmalonyl-Coenzyme A mutase deficiency   |   Mevalonate kinase deficiency   |   Mevalonicaciduria   |   Meyenburg-Altherr-Uehlinger syndrome   |   Michelin tire baby syndrome   |   Michels Caskey syndrome   |   Michels syndrome   |   Mickleson syndrome   |   Micrencephaly corpus callosum agenesis   |   Micrencephaly olivopontocerebellar hypoplasia   |   Micro syndrome   |   Microbrachycephaly ptosis cleft lip   |   Microcephalic osteodysplastic primordial dwarfism   |   Microcephalic primordial dwarfism   |   Microcephalic primordial dwarfism Toriello type   |   Microcephaly   |   Microcephaly albinism digital anomalies syndrome   |   Microcephaly autosomal dominant   |   Microcephaly brachydactyly kyphoscoliosis   |   Microcephaly brain defect spasticity hypernatremia   |   Microcephaly cardiac defect lung malsegmentation   |   Microcephaly cardiomyopathy   |   Microcephaly cervical spine fusion anomalies   |   Microcephaly chorioretinopathy recessive form   |   Microcephaly cleft palate autosomal dominant   |   Microcephaly deafness syndrome   |   Microcephaly developmental delay pancytopenia   |   Microcephaly facial clefting preaxial polydactyly   |   Microcephaly glomerulonephritis Marfanoid habitus   |   Microcephaly hiatus hernia nephrotic syndrome   |   Microcephaly hypergonadotropic hypogonadism short stature   |   Microcephaly immunodeficiency lymphoreticuloma   |   Microcephaly intracranial calcification   |   Microcephaly lymphoedema chorioretinal dysplasia   |   Microcephaly lymphoedema syndrome   |   Microcephaly mental retardation retinopathy   |   Microcephaly mental retardation spasticity epilepsy   |   Microcephaly mesobrachyphalangy tracheoesophageal fistula syndrome   |   Microcephaly microcornea syndrome Seemanova type   |   Microcephaly micropenis convulsions   |   Microcephaly microphthalmos blindness   |   Microcephaly nonsyndromal   |   Microcephaly pontocerebellar hypoplasia dyskinesia   |   Microcephaly seizures mental retardation heart disorders   |   Microcephaly sparse hair mental retardation seizures   |   Microcephaly syndactyly brachymesophalangy   |   Microcephaly with chorioretinopathy, autosomal dominant form   |   Microcephaly with normal intelligence, immunodeficiency   |   Microcephaly with spastic quadriplegia   |   Microcephaly, holoprosencephaly, and intrauterine growth retardation   |   Microcephaly, primary autosomal recessive   |   Microcoria, congenital   |   Microcornea corectopia macular hypoplasia   |   Microcornea glaucoma absent frontal sinuses   |   Microdontia hypodontia short stature   |   Microencephaly   |   Microgastria limb reduction defect   |   Microgastria short stature diabetes   |   Microinfarct   |   Micromelic dwarfism Fryns type   |   Micromelic dysplasia dislocation of radius   |   Microphobia   |   Microphtalmos bilateral colobomatous orbital cyst   |   Microphthalmia   |   Microphthalmia camptodactyly mental retardation   |   Microphthalmia cataract   |   Microphthalmia diaphragmatic hernia Fallot   |   Microphthalmia mental deficiency   |   Microphthalmia microtia fetal akinesia   |   Microphthalmia, Lentz type   |   Microphthalmos, microcornea, and sclerocornea   |   Microscopic polyangiitis   |   Microsomia hemifacial radial defects   |   Microspherophakia metaphyseal dysplasia   |   Microsporidiosis   |   Microtia, meatal atresia and conductive deafness   |   Microvillus Inclusion Disease   |   Miculicz syndrome   |   MIDAS syndrome   |   Midline cleft of lower lip   |   Midline defects autosomal type   |   Midline defects recessive type   |   Midline developmental field defects   |   Midline field defects   |   Midline lethal granuloma   |   Mietens syndrome   |   Mievis Verellen Dumoulin syndrome   |   Migraine   |   Mikulicz' Disease   |   Mikulicz Syndrome   |   Miller Fisher syndrome   |   Miller Syndrome   |   Miller-Dieker syndrome   |   Milner Khallouf Gibson syndrome   |   MILS syndrome   |   Minkowski-Chauffard disease   |   Minoxidil antenatal infection   |   Miosis, congenital   |   Mirror hands feet nasal defects   |   Mirror polydactyly segmentation and limbs defects   |   Misophobia   |   Mitochondrial cytopathy (generic term)   |   Mitochondrial Diseases   |   Mitochondrial diseases of nuclear origin   |   Mitochondrial diseases, clinically undefinite   |   Mitochondrial encephalomyopathy aminoacidopathy   |   Mitochondrial genetic disorders   |   Mitochondrial myopathy lactic acidosis   |   Mitochondrial myopathy-encephalopathy-lactic acidosis   |   Mitochondrial PEPCK deficiency   |   Mitochondrial trifunctional protein deficiency   |   Mitral atresia   |   Mitral regurgitation deafness skeletal anomalies   |   Mitral valve prolapse   |   Mitral Valve Prolapse Syndrome   |   Mitral valve prolapse, familial, autosomal dominant   |   Mitral valve prolapse, familial, X linked   |   Miura syndrome   |   Mixed Connective Tissue Disease (MCTD)   |   Mixed Mullerian tumor   |   Mixed sclerosing bone dystrophy   |   MLS syndrome   |   MMEP syndrome   |   MMT syndrome   |   MN1   |   MNGIE syndrome   |   Mobius syndrome   |   MODY syndrome   |   Moebius axonal neuropathy hypogonadism   |   Moebius Syndrome   |   Moerman Van den berghe Fryns syndrome   |   Moeschler Clarren syndrome   |   Mohr syndrome   |   Mohr-Tranebjaerg syndrome   |   Mollica Pavone Antener syndrome   |   Molluscum contagiosum   |   Moloney syndrome   |   Molybdenum cofactor deficiency   |   MOMO syndrome   |   Mondini Dysplasia   |   Mondor's disease   |   Monilethrix   |   Monoamine oxidase A deficiency   |   Monoclonal gammopathy of undetermined significance   |   Monodactyly tetramelic   |   Mononen Karnes Senac syndrome   |   Mononeuritis multiplex   |   Monosomy 8q12 21   |   Monosomy 8q21 q22   |   Monosomy X   |   Montefiore syndrome   |   Moore Federman syndrome   |   Moore Smith Weaver syndrome   |   Morel's ear   |   Moreno Zachai Kaufman syndrome   |   Morgani Turner Albright syndrome   |   Morhosseini Holmes Walton syndrome   |   Morillo Cucci Passarge syndrome   |   Morphea Scleroderma   |   Morphea, generalized   |   Morquio disease, type A   |   Morquio disease, type B   |   Morquio Syndrome   |   Morrison Young syndrome   |   Morse Rawnsley Sargent syndrome   |   Motor Neuron Disease   |   Motor neuro-ophthalmic disorders   |   Motor neuropathy   |   Motor neuropathy peripheral dysautonomia   |   Motor sensory neuropathy type 1 aplasia cutis congenita   |   Motorphobia   |   Mounier-Kuhn syndrome   |   Mount Reback syndrome   |   Mountain Sickness, Acute   |   Mousa Al din Al Nassar syndrome   |   Mowat-Wilson Syndrome   |   Moyamoya Syndrome   |   MPO deficiency   |   MPS III-A   |   MPS III-B   |   MPS III-C   |   MPS III-D   |   MPS VI   |   MR   |   MRKH Syndrome   |   MSBD syndrome   |   MTHFR deficiency   |   Mucha Habermann Disease   |   Muckle-Wells syndrome   |   Mucoepithelial dysplasia   |   Mucolipidosis IV   |   Mucolipidosis type 1   |   Mucolipidosis type 3   |   Mucopolysaccharidoses   |   Mucopolysaccharidosis type 4   |   Mucopolysaccharidosis Type I   |   Mucopolysaccharidosis type I Hurler/Scheie syndrome   |   Mucopolysaccharidosis type I Scheie syndrome   |   Mucopolysaccharidosis type II Hunter syndrome- mild form   |   Mucopolysaccharidosis type II Hunter syndrome- severe form   |   Mucopolysaccharidosis Type III   |   Mucopolysaccharidosis type IV-A Morquio syndrome   |   Mucopolysaccharidosis type IV-B   |   Mucopolysaccharidosis type V   |   Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate   |   Mucopolysaccharidosis type VII Sly syndrome   |   Mucosulfatidosis   |   Mucous Membrane Pemphigoid   |   Muenke Syndrome   |   Mulibrey Nanism syndrome   |   Mulibrey Nanism Syndrome (Perheentupa Syndrome)   |   Muller Barth Menger syndrome   |   Mullerian agenesis   |   Mullerian Aplasia   |   Mullerian derivatives lymphangiectasia polydactyly   |   Mullerian derivatives, persistent   |   Mullerian duct abnormalities galactosemia   |   Mulliez Roux Loterman syndrome   |   Multicentric osteolysis nephropathy   |   Multicentric reticulohistiocytosis   |   Multifocal heterotopia   |   Multifocal motor neuropathy with conduction block   |   Multifocal ventricular premature beats   |   Multinodular goiter cystic kidney polydactyly   |   Multiple acyl-CoA deficiency   |   Multiple carboxylase deficiency, biotin responsive   |   Multiple carboxylase deficiency, late onset   |   Multiple carboxylase deficiency, propionic acidemia   |   Multiple chemical sensitivity   |   Multiple congenital anomalies mental retardation, growth failure and cleft lip palate   |   Multiple congenital contractures   |   Multiple contracture syndrome Finnish type   |   Multiple endocrine neoplasia type 1   |   Multiple endocrine neoplasia, type 2   |   Multiple Epiphyseal Dysplasia   |   Multiple fibrofolliculoma familial   |   Multiple hereditary exostoses   |   Multiple joint dislocations metaphyseal dysplasia   |   Multiple myeloma   |   Multiple organ failure   |   Multiple pterygium syndrome   |   Multiple pterygium syndrome lethal type   |   Multiple Sclerosis   |   Multiple sclerosis ichthyosis factor VIII deficiency   |   Multiple subcutaneous angiolipomas   |   Multiple Sulfatase Deficiency   |   Multiple synostoses syndrome 1   |   Multiple System Atrophy   |   Multiple vertebral anomalies unusual facies   |   Mulvihill Smith Syndrome   |   Mumps   |   Munchausen by proxy syndrome   |   MURCS Association   |   Muscle-eye-brain syndrome   |   Muscular atrophy ataxia retinitis pigmentosa diabetes mellitus   |   Muscular dystrophy   |   Muscular dystrophy congenital infantile cataract hypogonadism   |   Muscular dystrophy congenital, merosin negative   |   Muscular dystrophy facioscapulohumeral   |   Muscular dystrophy Hutterite type   |   Muscular dystrophy limb girdle type 2A, Erb type   |   Muscular dystrophy limb-girdle autosomal dominant   |   Muscular dystrophy limb-girdle type 2B, Myoshi type   |   Muscular dystrophy limb-girdle with beta-sarcoglycan deficiency   |   Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency   |   Muscular dystrophy white matter spongiosis   |   Muscular Dystrophy, Becker   |   Muscular dystrophy, congenital, merosin-positive   |   Muscular Dystrophy, Duchenne   |   Muscular Dystrophy, Emery Dreifuss   |   Muscular Dystrophy, Limb Girdle   |   Muscular Dystrophy, Oculo Gastrointestinal   |   Muscular fibrosis multifocal obstructed vessels   |   Muscular phosphorylase kinase deficiency   |   Mutations in estradiol receptor   |   Mutism, Selective   |   Myalgia eosinophilia associated with tryptophan   |   Myalgic encephalomyelitis   |   Myasthenia Gravis   |   Myasthenia gravis congenital   |   Myasthenia, familial   |   Mycetoma   |   Mycobacterium avium complex infection   |   Mycophobia   |   Mycoplasmal pneumonia   |   Mycosis Fungoides   |   Mycosis fungoides lymphoma   |   Mycosis fungoides, familial   |   Mycositis fungoides   |   Myelinopathies   |   Myelitis   |   Myelocerebellar disorder   |   Myelodysplasia   |   Myelodysplastic Syndromes   |   Myelofibrosis   |   Myelofibrosis, Idiopathic   |   Myelofibrosis-osteosclerosis   |   Myeloid splenomegaly   |   Myeloma, Multiple   |   Myeloperoxidase deficiency   |   Myhre Ruvalcaba Graham syndrome   |   Myhre Ruvalcaba Kelley syndrome   |   Myhre School syndrome   |   Myhre Syndrome   |   Myoadenylate deaminase deficiency   |   Myocarditis   |   Myocardium disorder   |   Myoclonic dystonia   |   Myoclonic progressive familial epilepsy   |   Myoclonus ataxia   |   Myoclonus cerebellar ataxia deafness   |   Myoclonus epilepsy   |   Myoclonus epilepsy partial seizure   |   Myoclonus hereditary progressive distal muscular atrophy   |   Myoclonus progressive epilepsy of Unverricht and Lundborg   |   Myoclonus with epilepsy with ragged red fibers (mitochondria)   |   Myoclonus, General   |   Myofibrillar lysis   |   Myofibroblastic tumors   |   Myoglobinuria   |   Myoglobinuria dominant form   |   Myoglobinuria recurrent   |   Myoneurogastrointestinal encephalopathy syndrome   |   Myopathy   |   Myopathy and diabetes mellitus   |   Myopathy cataract hypogonadism   |   Myopathy congenital multicore with external ophthalmoplegia   |   Myopathy growth and mental retardation hypospadias   |   Myopathy Hutterite type   |   Myopathy mitochondrial cataract   |   Myopathy Moebius Robin syndrome   |   Myopathy ophthalmoplegia hypoacousia areflexia   |   Myopathy tubular aggregates   |   Myopathy with lactic acidosis and sideroblastic anemia   |   Myopathy with lysis of myofibrils   |   Myopathy, Congenital, Batten Turner Type   |   Myopathy, Desmin Storage   |   Myopathy, McArdle type   |   Myopathy, myotubular   |   Myopathy, Scapuloperoneal   |   Myopathy, X-linked, with excessive autophagy   |   Myophosphorylase deficiency   |   Myopia   |   Myopia, infantile severe   |   Myopia, severe   |   Myositis   |   Myositis ossificans   |   Myositis ossificans post-traumatic   |   Myositis ossificans progressiva   |   Myositis, Inclusion Body   |   Myotonia atrophica   |   Myotonia Congenita   |   Myotonia mental retardation skeletal anomalies   |   Myotubular Myopathy   |   Myxedema   |   Myxoid liposarcoma   |   Myxoma-spotty pigmentation-endocrine overactivity   |   Myxomatous peritonitis   |   Myxozoa   |