- List of diseases (M)
A list of
disease s in the English wikipedia.DiseasesTOC
Ma
Mac
*
Mac Ardle disease
*Mac Dermot Patton Williams syndrome
*Mac Dermot Winter syndrome Maci-Macr
*
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 Macu
*
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-Mag
*
Mad cow disease
*Madelung's disease
*Madokoro Ohdo Sonoda syndrome
*Maffucci syndrome
*Maghazaji syndrome
*Magnesium defect in renal tubular transport of
*Magnesium wasting renal Mal
*
Mal de debarquement Mala-Mall
*
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 Malo-Malp
*
Malonic aciduria
*Malonyl-CoA decarboxylase deficiency
*Malouf syndrome
*Malpuech facial clefting syndrome Man
*
Mandibuloacral dysplasia
*Mandibulofacial dysostosis deafness postaxial polydactyly
*Manic Depression, Bipolar
*Manic-depressive psychosis, genetic types
*Mannosidosis
*Manouvrier syndrome
*Mansonelliasis
*Mantle cell lymphoma Mar
Mara-Marg
*
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 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 Mari-Mart
*
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 Mas-May
*
MASA syndrome
*Mass syndrome
*Massa Casaer Ceulemans syndrome
*Mast cell disease
*Mastocytosis, short stature, hearing loss
*Mastocytosis
*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
*Mayer Rokitanski Kuster syndrome
*May-Hegglin Anomaly Mc
*
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 Me
Mea-Med
*
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 Meg-Mei
*
Megacystis microcolon intestinal hypoperistalsis syndrome
*Megaduodenum
*Mega-epiphyseal 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 Mel-Mem
*
Melanoma type 1
*Melanoma type 2
*Melanoma, familial
*Melanoma, Malignant
*Melanoma-astrocytoma syndrome
*Melanosis neurocutaneous
*MELAS
*Meleda Disease
*Melhem Fahl syndrome
*Melioidosis
*Melkersson-Rosenthal syndrome
*Melnick-Needles osteodysplasty
*Melnick-Needles syndrome
*Membranoproliferative glomerulonephritis (type II) Men
Mend-Meno
*
Mendelian susceptibility to atypical mycobacteria
*Menetrier's disease
*Mengel Konigsmark syndrome
* Ménière's disease
*Meningeal angiomatosis cleft hypoplastic left heart
*Meningioma 1
*Meningioma
*Meningitis, meningococcal
*Meningitis
*Meningocele
*Meningococcemia
*Meningoencephalocele
*Meningoencephalocele-arthrogryposis-hypoplastic thumb
*Meningomyelocele Ment
Menta
Mental
Mental d-Mental m
*Mental deficiency-epilepsy-endocrine disorders
*Mental mixed retardation deafnes clubbed digits Mental rMental retardation a-Mental retardation m
*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 n-Mental retardation s
*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 u-Mental retardation x
*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 Mer-Mes
* Mercury poisoning
*Meretoja syndrome
*Merkle tumors
*Merlob Grunebaum Reisner syndrome
*Merlob syndrome
*Mesangial sclerosis, diffuse
*Mesenteric ischemia
*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 Met
Meta
*
Metabolic acidosis
*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
*Metatrophic dysplasia
*Metatropic dwarfism Meth
*
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 Mev-Mey
*
Mevalonate kinase deficiency
*Mevalonicaciduria
*Meyenburg-Altherr-Uehlinger syndrome Mi
Mic
Mich-Mick
*
Michelin tire baby syndrome
*Michels Caskey syndrome
*Michels syndrome
*Mickleson syndrome Micr
Mircre
*
Micrencephaly corpus callosum agenesis
*Micrencephaly olivopontocerebellar hypoplasia Micro
*
Micro syndrome Microb
*
Microbrachycephaly ptosis cleft lip Microc
Microcephalic
*Microcephalic osteodysplastic primordial dwarfism
*Microcephalic primordial dwarfism Toriello type
*Microcephalic primordial dwarfism MicrocephalyMicrocephaly a-Microcephaly l
*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 m-Microcephaly w
*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 Microco
*Microcoria, congenital
*Microcornea corectopia macular hypoplasia
*Microcornea glaucoma absent frontal sinuses Microd-Microv
*
Microdontia hypodontia short stature
*Microencephaly
*Microgastria limb reduction defect
*Microgastria short stature diabetes
*Microinfarct
*Micromelic dwarfism Fryns type
*Micromelic dysplasia dislocation of radius
*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 Micu
*
Miculicz syndrome Mid-Mir
*
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-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 Mis-Mix
*
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 Müllerian tumor
*Mixed sclerosing bone dystrophy Ml-Mn
*
MLS syndrome
*MMEP syndrome
*MMT syndrome
* MN1
*MNGIE syndrome Mo
Mob-Mom
*
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 Mon-Moo
*
Mondini dysplasia
*Mondor's disease
*Monge'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 Mor-Moy
*
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
*Mounier-Kuhn syndrome
*Mount Reback syndrome
*Mousa Al din Al Nassar syndrome
*Moyamoya disease Mp-Mt
*
MPO deficiency
*MPS III-A
*MPS III-B
*MPS III-C
*MPS III-D
*MPS VI
*MRKH Syndrome (Mullerian Agenesis )
*MSBD syndrome
*MTHFR deficiency Mu
Muc-Mue
*
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 Mul
Muli-Mull
*
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 Mult
Multi
Multic-Multin
*
Multicentric osteolysis nephropathy
*Multicentric reticulohistiocytosis
*Multifocal heterotopia
*Multifocal motor neuropathy with conduction block
*Multifocal ventricular premature beats
*Multinodular goiter cystic kidney polydactyly Multip
Multiple a-Multiple p
*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 s-Multiple v
*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 Mum-Mut
*
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 My
Mya-Myc
*
Myalgia eosinophilia associated with tryptophan
*Myalgic encephalomyelitis
*Myasthenia gravis congenital
*Myasthenia gravis
*Myasthenia, familial
*Mycetoma
*Mycobacterium avium complex infection
*Mycoplasmal pneumonia
*Mycosis fungoides lymphoma
*Mycosis fungoides, familial
*Mycosis fungoides
*Mycositis fungoides Mye-Myi
*
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
*Myiasis Myo
Myoa-Myon
*
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 Myop
*
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, centronuclear
*Myopathy, desmin storage
*Myopathy, McArdle type
* Myopathy, myotubular
*Myopathy, X-linked, with excessive autophagy
*Myopathy
*Myophosphorylase deficiency
*Myopia
*Myopia, infantile severe
*Myopia, severe
* Myotubular myopathyMyos-Myot
*
Myositis ossificans post-traumatic
*Myositis ossificans progressiva
*Myositis ossificans
*Myositis, inclusion body
*Myositis
*Myotonia atrophica
*Myotonia mental retardation skeletal anomalies Myx
*
Myxedema
*Myxoid liposarcoma
*Myxoma-spotty pigmentation-endocrine overactivity
*Myxomatous peritonitis
*Myxozoa
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