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List of rare diseases starting with M
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This list of
rare diseases
was originally taken from the
NIH
public domain resource
at
http://ord.aspensys.com/diseases.asp
.
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Mac Dermot Patton Williams syndrome[?]
Mac Dermot Winter syndrome[?]
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 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 juvenile[?]
Macular degeneration, age-related[?]
Macular degeneration, polymorphic[?]
Macular degeneration[?]
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 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 hyperthermia[?]
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[?]
Marashi Gorlin syndrome[?]
Marchiafava Bignami disease[?]
Marchiafava-Micheli disease[?]
Marcus Gunn phenomenon[?]
Marden Walker like syndrome[?]
Marden-Walker syndrome[?]
Marek disease[?]
Marfan Syndrome type II[?]
Marfan Syndrome type III[?]
Marfan Syndrome type IV[?]
Marfan Syndrome type V[?]
Marfan syndrome
Marfan-like syndrome, Boileau type[?]
Marfan-Like syndrome[?]
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 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 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, short stature, hearing loss[?]
Mastocytosis
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[?]
Mayer Rokitanski Kuster syndrome[?]
May-Hegglin anomaly[?]
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[?]
Medium-chain Acyl-CoA dehydrogenase deficiency[?]
Medrano Roldan syndrome[?]
Medullary cystic disease[?]
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[?]
Meleda Disease[?]
Melhem Fahl syndrome[?]
Melkersson-Rosenthal syndrome[?]
Melnick-Needles osteodysplasty[?]
Melnick-Needles syndrome[?]
Melophobia[?]
Membranoproliferative glomerulonephritis (type II)[?]
Mendelian susceptibility to atypical mycobacteria[?]
Menetrier's disease[?]
Mengel Konigsmark syndrome[?]
Meniere's disease
Meningeal angiomatosis cleft hypoplastic left heart[?]
Meningioma 1[?]
Meningioma[?]
Meningitis, meningococcal[?]
Meningitis
Meningocele[?]
Meningococcemia[?]
Meningoencephalocele[?]
Meningoencephalocele-arthrogryposis-hypoplastic thumb[?]
Meningomyelocele[?]
Menophobia
Mental deficiency-epilepsy-endocrine disorders[?]
Mental mixed retardation deafnes clubbed digits[?]
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 bulbous nose[?]
Mental retardation epilepsy[?]
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 Ampola type[?]
Mental retardation unusual facies Davis Lafer type[?]
Mental retardation unusual facies talipes hand anomalies[?]
Mental retardation unusual facies[?]
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
Mental retardation-polydactyly-uncombable hair[?]
Mercury poisoning[?]
Meretoja syndrome[?]
Merkle tumors[?]
Merlob Grunebaum Reisner syndrome[?]
Merlob syndrome[?]
Mesangial sclerosis, diffuse[?]
Mesenteric panniculitis[?]
Mesodermal defects lower type[?]
Mesomelia synostoses[?]
Mesomelia[?]
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 disorder[?]
Metabolic Syndrome X[?]
Metacarpals 4 and 5 fusion[?]
Metachondromatosis[?]
Metageria[?]
Metaphyseal anadysplasia[?]
Metaphyseal chondrodysplasia Schmid type[?]
Metaphyseal chondrodysplasia Spahr type[?]
Metaphyseal chondrodysplasia, others[?]
Metaphyseal dysostosis mental retardation conductive deafness[?]
Metaphyseal dysplasia maxillary hypoplasia brachydactyly[?]
Metaphyseal dysplasia Pyle type[?]
Metastatic insulinoma[?]
Metatarsus adductus[?]
Metathesiophobia[?]
Metatrophic dysplasia[?]
Metatropic dwarfism[?]
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 with homocystinuria[?]
Methylmalonic acidemia[?]
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 Toriello type[?]
Microcephalic primordial dwarfism[?]
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[?]
Microcephaly
Microcoria, congenital[?]
Microcornea corectopia macular hypoplasia[?]
Microcornea glaucoma absent frontal sinuses[?]
Microdontia hypodontia short stature[?]
Microencephaly[?]
Microgastria limb reduction defect[?]
Microgastria short stature diabetes[?]
Micromelic dwarfism Fryns type[?]
Micromelic dysplasia dislocation of radius[?]
Microphobia[?]
Microphtalmos bilateral colobomatous orbital cyst[?]
Microphthalmia camptodactyly mental retardation[?]
Microphthalmia cataract[?]
Microphthalmia diaphragmatic hernia Fallot[?]
Microphthalmia mental deficiency[?]
Microphthalmia microtia fetal akinesia[?]
Microphthalmia, Lentz type[?]
Microphthalmia[?]
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[?]
Mikulicz' Disease[?]
Mikulicz syndrome[?]
Miller Fisher 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 of nuclear origin[?]
Mitochondrial diseases, clinically undefinite[?]
Mitochondrial Diseases
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, familial, autosomal dominant[?]
Mitral valve prolapse, familial, X linked[?]
Mitral valve prolapse[?]
Miura syndrome[?]
Mixed connective tissue disease[?]
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[?]
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 peripheral dysautonomia[?]
Motor neuropathy[?]
Motor sensory neuropathy type 1 aplasia cutis congenita[?]
Motorphobia[?]
Mounier-Kuhn syndrome[?]
Mount Reback syndrome[?]
Mousa Al din Al Nassar syndrome[?]
Moyamoya disease[?]
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 type 1[?]
Mucolipidosis type 3[?]
Mucolipidosis type 4[?]
Mucopolysaccharidosis type 3[?]
Mucopolysaccharidosis type 4[?]
Mucopolysaccharidosis type I Hurler syndrome[?]
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 IV-A Morquio syndrome[?]
Mucopolysaccharidosis type IV-B[?]
Mucopolysaccharidosis type V[?]
Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate[?]
Mucopolysaccharidosis type VII Sly syndrome
Mucopolysaccharidosis[?]
Mucosulfatidosis[?]
Muenke Syndrome[?]
Mulibrey Nanism 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 fibrofolliculoma familial[?]
Multiple hereditary exostoses[?]
Multiple joint dislocations metaphyseal dysplasia[?]
Multiple myeloma[?]
Multiple organ failure[?]
Multiple pterygium syndrome lethal type[?]
Multiple pterygium syndrome[?]
Multiple sclerosis ichthyosis factor VIII deficiency[?]
Multiple sclerosis
Multiple subcutaneous angiolipomas[?]
Multiple sulfatase deficiency[?]
Multiple synostoses syndrome 1[?]
Multiple system atrophy[?]
Multiple vertebral anomalies unusual facies[?]
Mumps
Munchausen by proxy syndrome[?]
Muscle-eye-brain syndrome[?]
Muscular atrophy ataxia retinitis pigmentosa diabetes mellitus[?]
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, congenital, merosin-positive[?]
Muscular dystrophy, Duchenne and Becker type[?]
Muscular dystrophy
Muscular fibrosis multifocal obstructed vessels[?]
Muscular phosphorylase kinase deficiency[?]
Mutations in estradiol receptor[?]
Myalgia eosinophilia associated with tryptophan[?]
Myalgic encephalomyelitis[?]
Myasthenia gravis congenital[?]
Myasthenia gravis
Myasthenia, familial[?]
Mycetoma[?]
Mycobacterium avium complex infection[?]
Mycophobia[?]
Mycoplasmal pneumonia[?]
Mycosis fungoides lymphoma[?]
Mycosis fungoides, familial[?]
Mycosis fungoides[?]
Mycositis fungoides[?]
Myelinopathies[?]
Myelitis
Myelocerebellar disorder[?]
Myelodysplasia
Myelodysplastic syndromes[?]
Myelofibrosis, idiopathic[?]
Myelofibrosis[?]
Myelofibrosis-osteosclerosis[?]
Myeloid splenomegaly[?]
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 partial seizure[?]
Myoclonus epilepsy[?]
Myoclonus hereditary progressive distal muscular atrophy[?]
Myoclonus progressive epilepsy of Unverricht and Lundborg[?]
Myoclonus with epilepsy with ragged red fibers (mitochondria)[?]
Myoclonus[?]
Myofibrillar lysis[?]
Myofibroblastic tumors[?]
Myoglobinuria dominant form[?]
Myoglobinuria recurrent[?]
Myoglobinuria[?]
Myoneurogastrointestinal encephalopathy syndrome[?]
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, desmin storage[?]
Myopathy, McArdle type[?]
Myopathy, myotubular[?]
Myopathy, X-linked, with excessive autophagy[?]
Myopathy[?]
Myophosphorylase deficiency[?]
Myopia, infantile severe[?]
Myopia, severe[?]
Myositis ossificans post-traumatic[?]
Myositis ossificans progressiva[?]
Myositis ossificans[?]
Myositis, inclusion body[?]
Myositis[?]
Myotonia atrophica[?]
Myotonia mental retardation skeletal anomalies[?]
Myxedema[?]
Myxoid liposarcoma[?]
Myxoma-spotty pigmentation-endocrine overactivity[?]
Myxomatous peritonitis[?]
Myxozoa[?]
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