1. Ma
    Mac  Maci–Macr  Macu  Mad–Mak  Mal  Mala–Mall  Malo–Malp  Man  Mar  Mara–Marg  Mari–Mart  Mas–May 

2. Mc

3. Me
    Mea–Med  Meg–Mei  Mel–Mem  Men  Mend–Meno  Ment  Menta  Mental  Mer–Mes  Met  Meta  Meth  Mev–Mey 

4. Mi
    Mib  Mic  Mich–Mick  Micr  Mircre  Micro  Microb  Microc  Microd – Microv  Micu  Mid–Mir  Mis–Mix 

5. Ml–Mn

6. Mo
    Mob–Mom  Mon–Moo  Mor–Moy 

7. Mp–Mt

8. Mu
    Muc–Mue  Mul  Muli–Mull  Mult  Multi  Multic–Multin  Multip  Mum–Mut 

9. My
    Mya–Myc  Mye–Myi  Myo  Myoa–Myon  Myop  Myos–Myot  Myx 

This is a list of diseases starting with the letter "M".

Ma

Mac

• 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
  • Macular degeneration juvenile
  • Macular degeneration, age-related
  • Macular degeneration, polymorphic
• Macular dystrophy, vitelliform
• Macules hereditary congenital hypopigmented and hyperpigmented

Mad–Mak

• Mad cow disease
• Madelung's disease
• Madokoro–Ohdo–Sonoda syndrome
• Maffucci syndrome
• Maghazaji syndrome
• Magnesium defect in renal tubular transport of
• Magnesium wasting renal
• Major depressive disorder

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
• 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 Müllerian 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
  • Marfan Syndrome type II
  • Marfan Syndrome type III
  • Marfan Syndrome type IV
  • Marfan Syndrome type V
• 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–Sjögren like syndrome
• Marinesco–Sjögren 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 psychogenic illness
• 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, names for:
  • Munchausen syndrome by proxy
  • Peripartum cardiomyopathy
• 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
• Mediastinal syndrome
• 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 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 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-polydactyly-uncombable hair

Mer–Mes

• Mercury poisoning (Mercurialism)
• 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 adenosyltransferase 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

Mib

• Mibies syndrome

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 osteodysplastic primordial dwarfism
• Microcephalic primordial dwarfism Toriello type
• Microcephalic primordial dwarfism

• 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 q­riplegia
• Microcephaly, holoprosencephaly, and intrauterine growth retardation
• Microcephaly, primary autosomal recessive

• Microcoria, congenital
• Microcornea correctopia 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
• Microphthalmia, Lentz type
• Microphthalmia camptodactyly mental retardation
• Microphthalmia cataract
• Microphthalmia diaphragmatic hernia Fallot
• Microphthalmia mental deficiency
• Microphthalmia microtia fetal akinesia
• Microphthalmia with limb anomalies
• 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 syndrome
• Mild cognitive impairment
• Miller Fisher syndrome
• Miller–Dieker syndrome
• Milner–Khallouf–Gibson syndrome
• MILS syndrome
• Minamata disease
• Minkowski–Chauffard syndrome
• Minoxidil antenatal infection
• Miosis, congenital
• Mirhosseini–Holmes–Walton syndrome
• 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 disease
• 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 receptive-expressive language disorder
• Mixed sclerosing bone dystrophy

Ml–Mn

• MLS syndrome
• MMEP syndrome
• MMT syndrome
• MN1
• MNGIE syndrome

Mo

Mob–Mom

• Möbius syndrome
• MODY syndrome
• Möbius axonal neuropathy hypogonadism
• Moerman Van den berghe Fryns syndrome
• Moeschler–Clarren syndrome
• Mohr syndrome
• Mohr–Tranebjærg 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
• 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 (Müllerian 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
• Mucormycosis
• Mucosulfatidosis
• Muenke syndrome

Mul

Muli–Mull

• Mulibrey nanism
• Müller–Barth–Menger syndrome
• Müllerian agenesis
• Müllerian aplasia
• Müllerian derivatives lymphangiectasia polydactyly
• Müllerian derivatives, persistent
• Müllerian duct abnormalities galactosemia
• Mulliez–Roux–Loterman syndrome

Mult

Multi

Multic–Multin

• Multicentric osteolysis nephropathy
• Multicentric reticulohistiocytosis
• Multifocal heterotopia
• Multifocal motor neuropathy
• Multifocal ventricular premature beats
• Multi-infarct dementia
• Multinodular goiter cystic kidney polydactyly

Multip

• 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

Mum–Mut

• Mumps
• Münchausen syndrome
• Münchausen syndrome by proxy
• 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
• Mycobacterium avium complex infection
• Mycoplasmal pneumonia
• Mycosis fungoides lymphoma
• Mycosis fungoides, familial
• Mycosis fungoides
• Mycositis fungoides

Mye–Myi

• Myelinopathy
• 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 epilepsy
• Myoclonic epilepsy with ragged red fibres (MERRF syndrome)
• Myoclonic progressive familial epilepsy
• Myoclonus ataxia
• Myoclonus cerebellar ataxia deafness
• Myoclonus epilepsy partial seizure
• Myoclonus hereditary progressive distal muscular atrophy
• Myoclonus progressive epilepsy of Unverricht and Lundborg
• 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 myopathy

Myos–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

• Owari-kuni
• Owari meisho zue
• Owari no Chronicle
• Owari no Seraph
• Owari Tokugawa Reimeikai Foundation
• Owari-Yokosuka Station
• Owasco Airport
• Owasco class cutter
• Owasco, Missouri
• Owasco, Nebraska
• Owasco Outlet
• OWASP ZAP
• Owasso High School
• Owasso Independent School District v Falvo
• Owasso Reporter
• Owata
• Owataria formosana
• Owata (Smashing Pumpkins song)
• Owata (The Smashing Pumpkins Song)
• Owata (The Smashing Pumpkins song)
• Owatonna Art Education Project
• Owatonna High School
• Owatonna, Minnesota micropolitan area
• Owatonna, MN Micropolitan Statistical Area
• Owatonna Senior High School